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Therapeutic Areas: Cardiology/Vascular Diseases | Hematology
Thromboembolism Clinical Trials
A listing of Thromboembolism medical research trials actively recruiting patient volunteers. Click on the closest city to find more detailed information on a research study in your area.
Alabama
Birmingham :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Montgomery : Baptist Health
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Arizona
Glendale : Arrowhead Hospital/Phoenix Heart, PLLC
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Arkansas
California
La Mesa :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Long Beach :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Modesto : Memorial Medical Center
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Orange : St. Joseph Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Palo Alto : Stanford University Medical Center
Treatment of Blood Clots in Children With Cancer
View More »
San Diego :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Stanford : Stanford University Medical Center
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Stanford :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Stanford : Stanford University Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Colorado
Wheat Ridge :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Connecticut
Danbury : Danbury Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Hartford : Hartford Hospital
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Norwich : Eastern Connecticut Hematology and Oncology Associates
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Delaware
Newark : Christiana Care Health Systems
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
District of Columbia
Florida
Bay Pines :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Clearwater :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Jacksonville :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Jacksonville : Nemours Children's Clinic/Jacksonville
Treatment of Blood Clots in Children With Cancer
Melbourne : Holmes Regional Medical Center
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
View More »
Orlando : Orlando Regional Medical Center
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Orlando : Florida Hospital
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Orlando : Florida Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Sarasota :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Tampa : Pepin Heart Hospital / University Community Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Tampa : St. Joseph's Children's Hospital of TampaPediatric Hematology/Oncology Research Department
Treatment of Blood Clots in Children With Cancer
Vero Beach :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Georgia
Atlanta : Emory University
Treatment of Blood Clots in Children With Cancer
Decatur :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Macon : Medical Center of Central Georgia
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Illinois
Chicago : University of Illinois at Chicago
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Chicago : Rush University Medical Center
Treatment of Blood Clots in Children With Cancer
Hinsdale : Adventist Midwest Health
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Oak Park :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Springfield : Prairie Heart Institue
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
View More »
Springfield : Southern Illinois University
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Winfield : Central DuPage Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Indiana
Carmel :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Indianapolis : St. Vincent Hospital
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Indianapolis : CorVasc
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Iowa
Iowa City : University of Iowa Carver's College of Medicine
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Windsor Heights :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Kansas
Topeka :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Kentucky
Florence : St. Elizabeth Healthcare of Northern Kentucky
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Lexington : University of Kentucky, Gill Heart Institute
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Louisvile : Kosair Charities Pediatric Clinical Research Unit- University of Louisville
Treatment of Blood Clots in Children With Cancer
Louisiana
New Orleans : East Jefferson General Hospital
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Maine
Portland : Maine Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Maryland
Annapolis :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Massachusetts
Boston : Massachusetts General Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Michigan
Ann Arbor : Ann Arbor Veteran's Administration Health System
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Ann Arbor : University of Michigan Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Detroit :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Detroit : Henry Ford Health System
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Detroit : Detroit Medical Center
Fondaparinux in Critically Ill Patients With Renal Failure
View More »
Southfield : Providence Hospital
AMPLATZER Cardiac Plug Clinical Trial
Minnesota
Duluth :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Rochester : Mayo Clinic
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Mississippi
Picayune :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Missouri
St. Louis :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
St. Louis : Washington University School of Medicine
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Montana
Butte :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Nebraska
Lincoln : Saint Elizabeth Regional Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Omaha :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Nevada
Reno :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
New Jersey
Morristown : Overlook Medical Center
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Teaneck : Holy Name Hospital
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Teaneck : Holy Name Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
New Mexico
Albuquerque : University of New Mexico
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Albuquerque : University of New Mexico
Treatment of Blood Clots in Children With Cancer
New York
Buffalo : Roswell Park Cancer Institute
A Study of Dalteparin Prophylaxis in High-Risk Ambulatory Cancer Patients
New York : Cornell Weill Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Rochester : University of Rochester Medical Center
A Study of Dalteparin Prophylaxis in High-Risk Ambulatory Cancer Patients
Rochester : Rochester General Hospital
A Study of Dalteparin Prophylaxis in High-Risk Ambulatory Cancer Patients
Staten Island :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Staten Island : Staten Island University Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
North Carolina
Chapel Hill : University of North Carolina at Chapel Hill
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Durham : Duke University School of Medicine
A Study of Dalteparin Prophylaxis in High-Risk Ambulatory Cancer Patients
Durham :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Durham : Duke University
Clinical Decision Rule Validation Study to Predict Low Recurrent Risk in Patients With Unprovoked Venous Thromboembolism
Durham : Duke Children's Hospital
Treatment of Blood Clots in Children With Cancer
View More »
Winston Salem : Wake Forest University Baptist Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Winston-Salem : Forsyth Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Ohio
Cincinatti : Good Samaritan Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Cleveland :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Cleveland : Cleveland Clinic
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Colombus : Univeristy Medical Center
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Columbus : Mt. Carmel East
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
View More »
Columbus : Riverside Methodist Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Toledo : Jobst Vascular Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Oregon
Portland : Oregon Health & Science University
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Portland : Oregon Health and Science University
Treatment of Blood Clots in Children With Cancer
Pennsylvania
Bethlehem : St. Luke's Hospital and Health Network
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Camp Hill :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Philadelphia : Albert Einstein Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Philadelphia : Temple University Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Pittsburgh : Allegheny General Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
View More »
Pittsburgh : The Western Pennsylvania Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Pittsburgh : University of Pittsburgh Medical Center Presbyterian Shadyside
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
West Reading : The Reading Hospital and Medical Center
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Rhode Island
Providence : Rhode Island Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
South Carolina
Charleston : Medical University of South Carolina
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Charleston : Medical Center of South Carolina
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Orangeburg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Tennessee
Memphis : St. Jude Children's Research Hospital
Treatment of Blood Clots in Children With Cancer
Texas
Bellaire :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Corsicana :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Dallas :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
El Paso : Providence Memorial and Sierra Medical Center
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Forth Worth : Cook Children's Medical Center
Treatment of Blood Clots in Children With Cancer
View More »
Houston : 1160.145.00001 Boehringer Ingelheim Investigational Site
Pharmacokinetics, Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
San Antonio :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Utah
Salt Lake City : University of Utah
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Virginia
Alexandria : Inova Alexandria Hospital
A Prospective, Single-arm, Multi-center Trial of EkoSonic® Endovascular System and Activase for Treatment of Acute Pulmonary Embolism (PE).
Charlottesville : University of Virginia Health System
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Richmond :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Washington
Tacoma : MultiCare Health System
A Phase 3, Randomized, Parallel-Group, Multi-Center, Multi-National Study for the Evaluation of Efficacy and Safety of (LMW) Heparin/Edoxaban Versus (LMW) Heparin/Warfarin in Subjects With Symptomatic Deep-Vein Thrombosis (DVT) and or Pulmonary Embolism (PE).
Wisconsin
Milwaukee : Medical College of Wisconsin/Froedtert Hospital
Acute Venous Thrombosis: Thrombus Removal With Adjunctive Catheter-Directed Thrombolysis
Australia
Herston :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Lismore :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Redcliffe :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Austria
Graz :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Graz : 1160.86.43001 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Wien :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Wien : 1160.84.4301 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
View More »
Wien : 1160.84.4310 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Wien : 1160.89.43001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Wien : 1160.86.43003 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Belgium
Brussel : 1160.89.32003 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Bruxelles :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Huy :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Leper :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Leuven :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Yvoir :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Brazil
Valinhos : LAL Clinica Pesquisa e Desenvolvimento Ltda
Efficacy And Safety Of Heparin In Patients With Cardiovascular Surgery Using Cardiopulmonary Bypass
Valinhos : LAL Clinica Pesquisa e Desenvolvimento Ltda
Efficacy And Safety Of Unfractionated Heparin In Patients With Cardiovascular Surgery Using Cardiopulmonary Bypass
Valinhos : Lal Clinica Pesquisa E Desenvolvimento Ltda
Efficacy of Sodium Heparin in Prophylaxis of Venous Thromboembolism in Surgical Patients
Bulgaria
Gabrovo :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Pleven :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Sofia :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Canada
Charlottetown : 1160.86.01003 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Edmonton : 1160.89.00002 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Halifax : QE II Health Sciences Centre
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Hamilton : Hamilton Health Sciences Corporation-General Hospital
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Hamilton : Hamilton Health Sciences Corporation-Henderson Site
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
View More »
Hamilton : Hamilton Health Sciences Corporation-McMaster Site
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Montreal : SMBD Jewish General Hospital
Clinical Decision Rule Validation Study to Predict Low Recurrent Risk in Patients With Unprovoked Venous Thromboembolism
Montreal : Montreal General Hospital
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Montreal : SMBD Jewish General Hospital
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Montréal : Maisonneuve Rosemont Hospital
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Oshawa : Isis Investigational Site
Active Comparator-Controlled Study to Assess Safety and Efficacy of ISIS FXI Rx in Total Knee Arthroplasty
Ottawa : Ottawa Hospital Research Institute (OHRI)
A Study of Dalteparin Prophylaxis in High-Risk Ambulatory Cancer Patients
Ottawa : Ottawa Health Research Institute
Clinical Decision Rule Validation Study to Predict Low Recurrent Risk in Patients With Unprovoked Venous Thromboembolism
Ottawa : Ottawa Hospital-General Campus
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Ottawa : 1160.89.00001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Ottawa : University of Ottawa Heart Institute
Strategy of Continued Versus Interrupted Dabigatran at Time of Device Surgery in Patients With Moderate to High Risk of Arterial Thromboembolic Events
Red Deer : 1160.86.01001 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Saskatoon : Saskatchewan Drug Research Institute
Clinical Decision Rule Validation Study to Predict Low Recurrent Risk in Patients With Unprovoked Venous Thromboembolism
Toronto : University Health Network - Toronto General Hospital
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Toronto : 1160.89.00005 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Vancouver : Diamond Health Care Centre
Long-Term Innohep® Treatment Versus a Vitamin K Antagonist (Warfarin) for the Treatment of Venous Thromboembolism (VTE) in Cancer
Croatia
Krapinske Toplice :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Rijeka :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Zagreb :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Czech Republic
Brno : 1160.86.42001 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Kyjov :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Liberec :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Litomysl :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Olomouc :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Olomouc : 1160.86.42003 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Ostrava :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Prague : 1160.86.42004 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Prague 5 : 1160.86.42002 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Praha 1 :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Praha 10 :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Usti nad Labem :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Zlin :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Denmark
Frederiksberg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Haderslev :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Hellerup :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Hillerod :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Hvidovre :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Kobenhavn NV :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Silkeborg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Slagelse :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Estonia
Tallinn :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Tartu :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
France
Angers : CHU d'Angers
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Angers : 1160.84.3311 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Angoulême : CH d'Angoulême
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Bois Guillaume Cédex : 1160.84.3318 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Bordeaux : 1160.84.3334 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
View More »
Brest :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Brest : HIA Clermont-Tonnerre
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Brest : Medical Intensive Care Unit
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Caen Cedex 5 : 1160.84.3303 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Castelnau Le Lez : Clinique du Parc CASTELNAU LE LEZ
National Evaluation of the Adherence to Recommendations of Venous Thrombo Embolism Treatment in Cancer Patients
Clermont-Ferrand cedex 1 : 1160.84.3314 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Corbeil Essonne : CH de Corbeil Essonne
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Creteil : 1160.84.3320 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Dijon : CHU de Dijon
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Dijon : University Hospital
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
DIJON Cédex : 1160.84.3307 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Grenoble : University Hospital
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Illkirch : 1160.84.3310 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Le Havre : 1160.84.3335 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Les Lilas : 1160.84.3326 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Lille cedex : 1160.84.3304 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Lyon : 1160.84.3312 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Marseille : 1160.84.3305 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Marseille : 1160.89.33002 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
MARSEILLE Cédex 05 : 1160.84.3330 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Metz : 1160.84.3325 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Montauban : CH Montauban
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Montauban : 1160.84.3333 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Morlaix : CH de Morlaix
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Nancy : Laboratoire d'Hémostase Hôpital de Brabois
Thromboprophylaxis and Bariatric Surgery
Nancy : Service de Chirurgie Digestive Hôpital de Brabois
Thromboprophylaxis and Bariatric Surgery
Nancy : Département d'Anesthésiologie Hôpital de Brabois
Thromboprophylaxis and Bariatric Surgery
Nantes : Service de chirurgie générale et digestive,Hôpital Hôtel Dieu
Thromboprophylaxis and Bariatric Surgery
Nantes Cédex 2 : 1160.84.3323 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Paris : Medical Intensive Care Unit
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Paris : 1160.84.3327 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Paris : 1160.84.3302 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Paris : 1160.84.3306 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Paris : 1160.89.33001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Paris cedex 10 : 1160.84.3309 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Pierre Bénite cedex : 1160.84.3313 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Poitiers : CHU de Poitiers
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Poitiers Cédex : 1160.84.3324 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Saint Etienne Cédex 2 : 1160.84.3322 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Saint Herblain Cédex : 1160.84.3321 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Saint Malo : CH de St Malo
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Saint Saulve : 1160.84.3319 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Strasbourg : Centre investigation Clinique Hôpital Civil
Thromboprophylaxis and Bariatric Surgery
Strasbourg : Clinique de l'Orangerie
Thromboprophylaxis and Bariatric Surgery
Strasbourg : Département d'Anesthésiologie Hôpital Civil
Thromboprophylaxis and Bariatric Surgery
Strasbourg : Laboratoire d'hémostase Hôpital de Hautepierre
Thromboprophylaxis and Bariatric Surgery
Strasbourg : Service de Chirurgie Digestive Hopital de Hautepierre
Thromboprophylaxis and Bariatric Surgery
Strasbourg : Service de Chirurgie Générale et Endocrinienne Hôpital Civil
Thromboprophylaxis and Bariatric Surgery
Toulouse Cedex 9 : 1160.84.3317 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Toulouse Cédex 9 : 1160.84.3316 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Tours : CHU de Tours
Efficacy of the Association Mechanical Prophylaxis + Anticoagulant Prophylaxis on Venous Thromboembolism Incidence in Intensive Care Unit (ICU)
Vannes Cédex : 1160.84.3332 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Germany
Berlin :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Bochum : 1160.84.04953 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Bonn :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Dresden :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Garmisch-Partenkirchen : 1160.84.04912 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
View More »
Gelnhausen : 1160.84.4922 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Magdeburg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Münster : 1160.84.04951 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Neuss :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Olsberg : 1160.84.04913 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Witten :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Zwickau : Heinrich-Braun-Klinikum Zwickau gemeinnützige GmbH
Management and Detection of Atrial Tachyarrhythmias in Patients Implanted With BIOTRONIK DX Systems
Hungary
Balassagyarmat :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
India
Hyderabad : Care Hospital
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
New Delhi : Sir Ganga Ram Hospital
PERIOP 2 - A Safety and Effectiveness Study of LMWH Bridging Therapy Versus Placebo Bridging Therapy for Patients on Long Term Warfarin and Require Temporary Interruption of Their Warfarin.
Israel
Afula :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Ashkelon :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Haifa :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Holon :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Jerusalem :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Kfar Saba :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Nahariya :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Safed :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Tel Aviv :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Zerifin :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Italy
Bollate :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Bologna : University Hospital
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Castelfranco Veneto :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Latina : 1160.84.03908 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Milan : IRCCS H San Raffaele
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
View More »
Milano :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Milano : 1160.84.03902 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Monza : 1160.84.03904 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Monza : 1160.84.03903 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Parma :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Piacenza :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Roma :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Roma : 1160.89.39001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Udine : 1160.84.03909 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Varese :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Vittorio Veneto TV :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Korea, Republic of
Many Locations :
Xarelto Regulatory Post-Marketing Surveillance
Latvia
Daugavpils :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Liepaja :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Riga :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Riga : 1160.89.37101 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Valmiera :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Lithuania
Kaunas :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Klaipeda :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Siauliai :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Vilnius :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Vilnius : 1160.89.37001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Netherlands
Nijmegen : 1160.89.31003 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Utrecht : 1160.89.31004 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Norway
Bergen : 1160.89.47001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Poland
Bialystok :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Bydgoszcz :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Czeladz :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Gdansk :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Krakow :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Skierniewice :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Tarnobrzeg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Warszawa :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Russian Federation
Kemerovo :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Samara :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
St. Petersburg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Yaroslavl :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Singapore
Singapore :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
South Africa
Cape Town :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Johannesburg :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Spain
Alicante : University Hospital
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Badalona (Barcelona) : 1160.84.3409 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Barcelona :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Barcelona : 1160.84.3410 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
L'Hospitalet de Llobregat :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
View More »
Linares, Jaén : 1160.84.3413 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Madrid :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Madrid :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Madrid : 1160.84.3408 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Madrid : 1160.84.3403 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Madrid : 1160.89.34001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Madrid : 1160.89.34002 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Majadahonda :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Malaga : 1160.84.3405 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Orihuela :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Pamplona : 1160.84.3404 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Pozuelo de Alarcón - Madrid : 1160.84.3412 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Sabadell :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
San Sebastián de los Reyes :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Sant Boi de Llobregat :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Soria : General Hospital
STA®-Liatest®D-Di-Exclusion of Venous Thromboembolism
Tarragona :
Acute Medically Ill VTE Prevention With Extended Duration Betrixaban Study (The APEX Study)
Valencia : 1160.84.3411 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Valencia : 1160.84.3401 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Zaragoza : 1160.84.3402 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Sweden
Hässleholm : 1160.86.46002 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Kungälv : 1160.84.4603 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Mölndal : 1160.86.46001 Boehringer Ingelheim Investigational Site
Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate
Motala : 1160.84.4601 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
View More »
Stockholm : Karolinska University Hospital
Compression Treatment Effects on Complications and Healing of Achilles Tendon Rupture
Switzerland
Geneva : Hopitaux Universitaires de Geneve
Clinical Decision Rule Validation Study to Predict Low Recurrent Risk in Patients With Unprovoked Venous Thromboembolism
Many Locations :
Treatment of an Acute Deep Vein Thrombosis (DVT) With Either Rivaroxaban or Current Standard of Care Therapy
Zürich : 1160.89.41001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Thailand
Bangkok : 1160.89.66001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Ukraine
Dnipropetrovsk : 1160.89.38001 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Lugansk : 1160.89.38002 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
Vinnytsya : 1160.89.38003 Boehringer Ingelheim Investigational Site
Safety and Tolerability of Dabigatran Etexilate Solution in Children 1 to < 12 Years of Age
United Kingdom
Basildon : 1160.84.04405 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Bedford : 1160.84.04408 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Luton : 1160.84.04403 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Wigan : 1160.84.04401 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery
Yeovil : 1160.84.04407 Boehringer Ingelheim Investigational Site
Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery