Overview

Effects of Low Molecular Weight Heparin Versus Dabigatran on Platelet Aggregation in Patients With Stable Coronary Artery Disease

Status:
Completed
Trial end date:
2015-11-01
Target enrollment:
0
Participant gender:
All
Summary
Anticoagulation with heparin is indicated in several situations, such as acute coronary disease (in combination with antiplatelet therapy) for the prevention and treatment of venous thromboembolism and situations with high risk of thromboembolism. Recently, the latest trials on anticoagulation for stroke prevention on atrial fibrillation have shown an increased risk for acute mycardial infarction on patients submitted to new oral anticoagulants, such as dabigatran. The mechanism is still unclear, however, in this context, some previous studies about interaction between anticoagulants ( mainly heparin) and platelet aggregation have shown conflicting results: while some suggest an inhibitory effect of heparin on platelet function, others suggest that heparin could promote an increase in platelet activation. The present study aims to assess the effects of the LMWH Enoxaparin and direct thrombin inhibitor, Dabigatran, on platelet aggregation, studied and compared by different methods in patients with chronic coronary artery disease (CAD).
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
University of Sao Paulo General Hospital
Collaborator:
Fundação de Amparo à Pesquisa do Estado de São Paulo
Treatments:
Dabigatran
Dalteparin
Enoxaparin
Heparin, Low-Molecular-Weight
Criteria
Inclusion Criteria:

Age > 18 years old Coronary artery disease, defined as previous myocardial infarction
and/or coronary angioplasty and/or Coronary Artery Bypass Graft (CABG) surgery and/or
coronariography showing obstruction of at least 50 % in one of major epicardial vessels
Treatment with Acetylsalicylic Acid (ASA) 100 mg/day

Exclusion Criteria:

Use in the last 7 days of oral anticoagulant or any other antiplatelet drug beside ASA
Active bleeding Pregnancy or woman of childbearing age without contraceptive method
Hemoglobin < 10 g/dL or hematocrit < 30 %, hematocrit > 50 %, platelets < 100.000/mm3 or >
500.000/mm3; creatinin clearance < 50 ml/minute Percutaneous coronary intervention (PCI) on
the last 30 days before randomization (or PCI on the last year when drug-eluted stents are
used); CABG surgery on the last 90 days; acute coronary syndrome on the last 60 days Active
malignant neoplasm Active peptic ulcer disease on the last 60 days or upper
gastrointestinal bleeding any time in life Refuse to participate in the study