Clinical trial Recruiting at 1 site Observational Ages 16 and up

Identifying factors that predict survival and neurological outcomes in patients treated with E-CPR.

Official title: Predictors for Survival and Good Neurological Outcome in E-CPR and Non CPR Treated Patients

Run by Sahlgrenska University Hospital · NCT04198792 · Data updated 2026-11-12

This study looks at patients who received ECMO treatment after a cardiac arrest to see what factors can help predict their survival and brain recovery.

Quick facts

Study typeObservational
Ages16 Years and up
SexAll
Enrollment700 (estimated)
SponsorSahlgrenska University Hospital
Academic / other
Locations1 site (Gothenburg)
StatusRecruiting
StartedJanuary 1, 2010
Main results expectedJanuary 1, 2030
Study endsJanuary 1, 2030
Registry record updatedJanuary 20, 2026
Trial IDNCT04198792 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates for this study are patients treated with ECMO at Sahlgrenska University Hospital following cardiac arrest.

Probably not a fit

Patients who do not receive ECMO treatment or those with severe pre-existing neurological conditions may 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 focuses on patients who have undergone extracorporeal membrane oxygenation (ECMO) treatment after cardiac arrest. It aims to identify predictors of good neurological outcomes by analyzing data from the Gothenburg ECPR cohort. The study will assess the effectiveness of pre-primed ECMO circuits and evaluate the current neurological prognostication guidelines for comatose patients. Additionally, long-term follow-up will be conducted to understand the neuropsychological outcomes and life satisfaction of ECPR survivors.

Why it matters

Potential benefit: If successful, this study could lead to improved patient selection for ECPR, enhancing survival rates and neurological outcomes for cardiac arrest patients.

How similar studies have gone: Other studies have shown success in refining patient selection criteria for ECMO, but this specific approach is novel in its focus on ECPR outcomes.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* ECMO-treated patients.

Exclusion Criteria:

* None

Where it's running

  • Sahlgrenska Academy at Sahlgrenska University Hospital
    Gothenburg, Sweden
    Recruiting

Study contacts

  • Principal investigator: Bengt Redfors, MD, PhD — The Sahlgrenska Academy ar Sahlgrenska University Hospital, Gorhenburg, Sweden
  • Study coordinator: Bengt Redfors, MD, PhD
  • Email: bengt.redfors@vgregion.se
  • Phone: +46768445402

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.