The project's main goal is to collect baseline clinical and procedural data as well as to assess clinical outcomes for all patients undergoing ECMO or Impella implantation at all included sites. All patients undergoing ECMO and/or IMPELLA implantation will be prospectively registered. Device use is according to the decision of the treating physician and independent of this registry.
| Facility | City | Region | Status |
|---|---|---|---|
| Universitätsspital Basel | Basel | Switzerland | Recruiting |
| Insel Gruppe AG, Inselspital Bern | Bern | Switzerland | Recruiting |
| Luzerner Kantonsspital | Lucerne | Switzerland | Recruiting |
| Kantonsspital Winterthur | Winterthur | Switzerland | Recruiting |
| Stadtspital Treimli | Zurich | Switzerland | Recruiting |
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04117230 on ClinicalTrials.gov ↗ ← All trials in Switzerland