Recombinant vWF Concentrate and ECMO

Recruiting Phase 1 Interventional Study
Bleeding Disorder
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
12 (estimated)
Sponsor
University of Virginia · Other
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About This Trial
Adult patients on extracoporeal membrane oxygenation (ECMO) frequently experience bleeding, which is in part caused by acquired von Willebrand syndrome (vWS). Prior in vitro studies have shown that the addition of recombinant von Willebrand Factor (vWF) to ECMO patient blood samples, normalizes platelet adhesion and thrombus formation. This study is a phase I study, where adult ECMO patients with …
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Adult patients (18 years or greater) 2. On extracorporeal membrane oxygenation 3. Major bleeding defined by CTCAE class 3 or greater 4. Off systemic anticoagulation for at least 4 hours Exclusion Criteria: 1. Platelet count less than 40 x 109/L 2. International normalized r…
Contacts

Michael Mazzeffi, MD

434-924-9520

syy4wa@uvahealth.org

CONTACT

Keita Ikeda, PhD

434-924-2283

KI2D@uvahealth.org

CONTACT