Overview

Comparison of Anticoagulation Prolongation vs. no Anticoagulation in STEMI Patients After Primary PCI

Status:
Recruiting
Trial end date:
2022-12-01
Target enrollment:
Participant gender:
Summary
The RIGHT study is a large randomized study dedicated to post-PPCI anticoagulation in STEMI patients. The investigators propose to evaluate the clinical efficacy and safety of anticoagulation prolonged for at least 48 hours after the procedure vs. no prolongation of anticoagulation after procedure in patients with STEMI treated with bivalirudin during PPCI (primary hypothesis). When allocated to anticoagulation prolongation by randomization, the subject will be assigned to UFH, enoxaparin or bivalirudin (same regimen allocated by centre) for at least 48 hours after PPCI. The results from this study are expected to provide guidance on the risk/benefit of post-procedural anticoagulation in patients with STEMI.
Phase:
Phase 4
Details
Lead Sponsor:
Beijing Anzhen Hospital
Collaborators:
ACTION Study Group (Pitié-Salpêtrière Hospital), Paris, France
Chinese Academy of Medical Sciences, Fuwai Hospital
Treatments:
Bivalirudin
Calcium heparin
Enoxaparin
Enoxaparin sodium
Heparin
Hirudins