The ECMO-Free Trial
Trial ID or NCT#
Status
Purpose
Decannulation from venovenous extracorporeal membrane oxygenation (VV-ECMO) at the earliest and safest time would be expected to improve outcomes and reduce cost. Daily assessments for readiness to liberate from therapies have demonstrated success in other realms of critical care. A recent single-center study demonstrated that a protocolized daily assessment of readiness for liberation from VV-ECMO was feasible and did not raise any major safety concerns, but the effect of this protocolized daily assessment on clinical outcomes remains unclear. Further, the manner in which ECMO is provided, weaned, and discontinued varies significantly between centers, raising persistent concerns regarding widespread adoption of protocolized daily assessment of readiness for liberation from VV-ECMO. Data from large a randomized controlled trial is needed to compare the effects of a protocolized daily assessment of readiness for liberation from VV-ECMO versus usual care on duration of ECMO support and other clinical outcomes.
Official Title
ECMO-Free Trial: A Multicenter Randomized Controlled Trial
Eligibility Criteria
- * Patient receiving VV-ECMO* Patient is located in a participating unit of an adult hospital
- * Patient is pregnant* Patient is a prisoner* Patient is \< 18 years old* Participant is receiving ECMO as bridge to transplant* Participant is receiving a hybrid configuration that includes an arterial cannula* Patient has received VV-ECMO for \> 48 hours
Investigator(s)
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Contact
Whitney D Gannon, MSN, MS
6109095789
View on ClinicalTrials.gov