Clinical trial Recruiting at 1 site Observational Ages 18 and up

Evaluating outcomes and quality of life for patients on ECMO

Official title: ESTimation of Outcome by Health-Care PRoviders Compared With TruE Outcome in Patients Undergoing Veno-arteriaL and Veno-venous ExtracorporeaL MembrAne Oxygenation

Run by Heinrich-Heine University, Duesseldorf · NCT06400797 · Data updated 2026-11-12

This study is trying to see how well patients do and how their quality of life is after receiving ECMO therapy for serious breathing or heart problems.

More Extracorporeal Membrane Oxygenation trials

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment1000 (estimated)
SponsorHeinrich-Heine University, Duesseldorf
Academic / other
Locations1 site (Düsseldorf, North Rhine-Westphalia)
StatusRecruiting
StartedJanuary 1, 2024
Main results expectedJanuary 1, 2028
Study endsJanuary 1, 2029
Registry record updatedMay 6, 2024
Trial IDNCT06400797 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are adults aged 18 and older who are starting ECMO therapy within 24 hours and can provide informed consent.

Probably not a fit

Patients under 18 years old, those who cannot communicate in the required languages, or those who have not undergone ECMO therapy will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to assess the outcomes and quality of life for patients undergoing extracorporeal membrane oxygenation (ECMO) therapy for severe respiratory or cardiocirculatory failure. It will compare healthcare providers' estimated outcomes with actual patient results to better understand the effectiveness of ECMO treatment. The study focuses on long-term implications of ECMO, particularly regarding quality of life after hospital discharge, which has been insufficiently studied. By gathering data on patient-centered outcomes, the research seeks to improve decision-making processes in emergency ECMO situations.

Why it matters

Potential benefit: If successful, this study could provide valuable insights into the long-term quality of life for ECMO patients, leading to improved treatment decisions and patient care.

How similar studies have gone: While there is limited data on long-term quality of life for ECMO patients, this study addresses a gap in existing research, making it a novel approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* age ≥ 18 years
* start of ECMO therapy ≤24h
* written informed consent from patient or health-care proxy

Exclusion Criteria:

* age \< 18 years
* Language barrier (communication in German/local language or English not possible).
* no ECMO therapy or ECMO therapy longer than 24h
* no written consent

Where it's running

  • University Hospital Duesseldorf
    Düsseldorf, North Rhine-Westphalia, Germany
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.