drugset / Trial / NCT03568838

Prolonged Enoxaparin in Primary Percutaneous Coronary Intervention

NCT03568838

RandomizedParallel-groupOpen-labelPrevention

Summary

This is a feasibility study aiming to generate pilot data on safety and efficacy of a novel anticoagulant regimen (enoxaparin bolus and prolonged infusion) compared to the local standard-of-care in opiate-treated patients undergoing primary percutaneous coronary intervention.

Timeline

Start
2018-06-28
Primary completion
2020-05-01
Completion
2020-05-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Enoxaparin sodium Other / unclassified 0.75 mg/kg Intravenous

Indications