Bivalirudin vs Heparin in ECMO Patients
Withdrawn before enrolling · Phase 1
Conditions studied: Extracorporeal Membrane Oxygenation Complication
In brief
This is an open label, randomized study comparing the clinical outcomes of unfractionated Heparin and Bivalirudin for anticoagulation in adult subjects requiring ECMO support.
Key facts
- Study ID
- NCT03707418
- Run by
- Johns Hopkins University
- People needed
- 0
- Starts
- 2021-04-01
- Expected to finish
- 2021-06-01
- Last updated by the study team
- 2021-01-19
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult patients on veno-arterial (VA) or veno-venous (VV)ECMO
You may not qualify if…
- Patient or surrogate decision makers cannot provide informed consent.
- Patients who have intolerance to either heparin or bivalirudin
- Patients who received any form of thrombolytic therapy within the past 30 days.
Where it is running
- Johns Hopkins University — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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