The ECMO-Free Trial

Trial ID or NCT#

NCT05486559

Status

recruiting iconRECRUITING

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

Ages Eligible for Study: Older than 18
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. * Patient receiving VV-ECMO* Patient is located in a participating unit of an adult hospital
Exclusion Criteria:
  1. * 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)

Melissa Ann Vogelsong
Clinical Associate Professor, Anesthesiology, Perioperative and Pain Medicine
Vikram Fielding-Singh, MD, JD
Clinical Associate Professor, Anesthesiology, Perioperative and Pain Medicine

Contact us to find out if this trial is right for you.

Contact

Whitney D Gannon, MSN, MS
6109095789