RECRUITINGOBSERVATIONAL
CARDSUP - SWISS Circulatory Support Registry
Clinical Outcomes in Patients in Need of a Non-permanent Extracorporeal Cardiocirculatory Support System (Peripheral Extracorporeal Membrane Oxygenation (ECMO) or Axial Flow Pump IMPELLA)
About This Trial
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.
Who May Be Eligible (Plain English)
Who May Qualify:
- Age \> 18 years
- Medical indication for implantation of a peripheral cannulated VA-ECMO or microaxial flow pump (IMPELLA) or newer LV / LA-Ascending Aorta devices.
- Signed willing to sign a consent form by patient or relative or waived consent by EC
Who Should NOT Join This Trial:
- None
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Age \> 18 years
* Medical indication for implantation of a peripheral cannulated VA-ECMO or microaxial flow pump (IMPELLA) or newer LV / LA-Ascending Aorta devices.
* Signed informed consent by patient or relative or waived consent by EC
Exclusion Criteria:
* None
Locations (5)
Universitätsspital Basel
Basel, Switzerland
Insel Gruppe AG, Inselspital Bern
Bern, Switzerland
Luzerner Kantonsspital
Lucerne, Switzerland
Kantonsspital Winterthur
Winterthur, Switzerland
Stadtspital Treimli
Zurich, Switzerland