Last updated: December 12, 2005
Sponsor: PAMI Coordinating Center
Overall Status: Trial Status Unknown
Phase
N/A
Condition
Blood Clots
Congestive Heart Failure
Hypercholesterolemia
Treatment
N/AClinical Study ID
NCT00136929
HIC 1999-225
Ages > 70 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age >= 70
Clinical symptoms > 30 minutes
Symptom onset <= 12 hours
ST segment elevation >= 1 mm in 2 or more leads
Exclusion
Exclusion Criteria:
Prior thrombolytics
Cardiogenic shock
Cerebrovascular accident (CVA)
Prolonged cardiopulmonary resuscitation (CPR)
Blood pressure (BP) > 180/100 mm Hg
Active bleeding
International Normalized Ratio (INR) > 1.4
Acetylsalicylic acid [aspirin] (ASA) or heparin allergy
History of neutropenia, thrombocytopenia, hepatic dysfunction, or renal insufficiency
Peripheral vascular disease (PVD)
Study Design
Total Participants: 530
Study Start date:
Estimated Completion Date: