drugset / Trial / NCT03568838
Prolonged Enoxaparin in Primary Percutaneous Coronary Intervention
Phase 4
Completed
100 enrolled
Sheffield Teaching Hospitals NHS Foundation Trust
Medical Research Council · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Enoxaparin sodium | Other / unclassified | 0.75 mg/kg | Intravenous |