Panama, Panama Clinical Trials

A listing of Panama, Panama clinical trials actively recruiting patients volunteers.

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Found 18 clinical trials
VenTouch OUS Feasibility Study

This is a prospective, multi-center, single-arm study to evaluate safety and efficacy of the VenTouch System for treatment of subjects with functional MR.

London Health Sciences Centre, University Hospital
 (2342.9 away) Contact site
  • 5 views
  • 25 Jan, 2021
  • +14 other locations
CPNS Pilot Study: Evaluation of Safety and Performance of the Cardiac Pulmonary Nerve Stimulation (CPNS) System in Patients With ADHF

The CPNS Pilot Study: An evaluation of the safety and performance of the Cardionomic Cardiac Pulmonary Nerve Stimulation (CPNS) system in patients with acute decompensated heart failure.

The Christ Hospital
 (2097.6 away) Contact site
  • 0 views
  • 22 Sep, 2021
  • +5 other locations
Study Evaluating Pharmacokinetics (PK) Safety and Efficacy of Cobicistat-boosted Atazanavir (ATV/co) or Cobicistat-boosted Darunavir (DRV/co) and Emtricitabine/Tenofovir Alafenamide (F/TAF) in HIV-1 Infected Virologically Suppressed Pediatric Participants

Cohort 1: The primary objectives are: To evaluate the steady-state pharmacokinetics (PK) of Atazanavir (ATV) and Darunavir (DRV) and confirm the dose of Cobicistat-boosted Atazanavir (ATV/co) or Cobicistat-boosted Darunavir (DRV/co) in HIV-1 infected, virologically suppressed adolescent participants weighing 25 kg (12 to < 18 years of age) To evaluate the …

ritonavir
emtricitabine/tenofovir
antiretroviral agents
atazanavir
tenofovir
University of South Florida
 (1317.7 away) Contact site
  • 236 views
  • 21 Aug, 2021
  • +40 other locations
Brief Title: Study of Efficacy and Safety of Canakinumab as Adjuvant Therapy in Adult Subjects With Stages AJCC/UICC v. 8 II-IIIA and IIIB (T>5cm N2) Completely Resected Non-small Cell Lung Cancer Acronym: CANOPY-A

The primary purpose of the study is to compare the efficacy and safety of canakinumab versus placebo as adjuvant therapy in adult subjects with stages AJCC/UICC v. 8 II -IIIA and the subset of IIIB (T>5cm N2 disease) completely resected (R0) non-small cell lung cancer (NSCLC).

systemic therapy
lung carcinoma
alopecia
Novartis Investigative Site
 (248.2 away) Contact site
  • 645 views
  • 21 Sep, 2021
  • +416 other locations
The Effect of Higher Protein Dosing in Critically Ill Patients

The investigator will investigate the effects of higher protein/amino acid dosing (2.2 g/kg/d) vs usual protein/amino acid dosing (1.2 g/kg/d) on clinical outcomes in nutritionally high risk ill patients.

amino acids
severe malnutrition
sarcopenia
Hospital Irma De Lourdes Tzanetatos
 (0.6 away) Contact site
  • 123 views
  • 02 Jul, 2021
  • +93 other locations
Hokusai Study in Pediatric Patients With Confirmed Venous Thromboembolism (VTE)

This is an event driven Phase 3, prospective, randomized, open-label, blinded endpoint evaluation (PROBE) parallel group study in subjects with confirmed VTE. This study is designed to evaluate the pharmacokinetics (PK) and pharmacodynamics (PD) of edoxaban and to compare the efficacy and safety of edoxaban against standard of care in …

heparin
vitamin k antagonist
anticoagulants
edoxaban
probe
Hospital Nacional de Ni os Benjam n Bloom
 (730.2 away) Contact site
  • 0 views
  • 28 Jan, 2021
  • +169 other locations
Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infections in Children Known or Suspected to be Caused by Susceptible Gram-positive Organisms Including MRSA

To determine the safety and descriptive efficacy of dalbavancin for the treatment of acute bacterial skin and skin structure infections in children, aged birth to 17 years (inclusive), known or suspected to be caused by susceptible Gram-positive organisms, including methicillin-resistant strains of Staphylococcus aureus.

pustular folliculitis
wound infection
induration
surgical incision
methicillin
Hospital Materno Infantil Jos Domingo de Obald a
 (197.0 away) Contact site
  • 0 views
  • 24 Jan, 2021
  • +95 other locations
A Study to Evaluate the Safety and Efficacy of MEDI8897 for the Prevention of Medically Attended RSV LRTI in Healthy Late Preterm and Term Infants

The purpose of this study is to evaluate the efficacy, safety, pharmacokinetics (PK), and antidrug antibody (ADA) response for MEDI8897 in healthy late preterm and term infants who are 35 weeks or greater gestational age and entering their first RSV season.

Research Site
 (18.6 away) Contact site
  • 580 views
  • 22 Sep, 2021
  • +414 other locations
Study of Two Doses of Crizanlizumab Versus Placebo in Adolescent and Adult Sickle Cell Disease Patients

The purpose of this study is to compare the efficacy and safety of 2 doses of crizanlizumab (5.0 mg/kg and 7.5 mg/kg) versus placebo in adolescent and adult sickle cell disease (SCD) patients with history of vaso-occlusive crisis (VOC) leading to healthcare visit.

acute chest syndrome
glutamine
priapism
acute pain
opioid
Novartis Investigative Site
 (248.2 away) Contact site
  • 100 views
  • 22 Sep, 2021
  • +88 other locations
Study Exploring the Effect of Crizanlizumab on Kidney Function in Patients With Chronic Kidney Disease Caused by Sickle Cell Disease

The goal of the study is to compare the efficacy and safety of crizanlizumab + standard of care to standard of care alone on renal function in sickle cell disease patients 16 years with chronic kidney disease due to sickle cell nephropathy.

thal
conjugated bilirubin
hydroxyurea
absolute neutrophil count
University of Florida
 (1436.4 away) Contact site
  • 7 views
  • 19 Sep, 2021
  • +30 other locations