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 type | Observational |
|---|---|
| Ages | 16 Years and up |
| Sex | All |
| Enrollment | 700 (estimated) |
| Sponsor | Sahlgrenska University Hospital Academic / other |
| Locations | 1 site (Gothenburg) |
| Status | Recruiting |
| Started | January 1, 2010 |
| Main results expected | January 1, 2030 |
| Study ends | January 1, 2030 |
| Registry record updated | January 20, 2026 |
| Trial ID | NCT04198792 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
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.