Clinical Outcomes in Patients in Need of a Non-permanent Extracorporeal Cardiocirculatory Support System (Peripheral Extracorporeal Membrane Oxygenation (ECMO) or Axial Flow Pump IMPELLA)
Status: Recruiting
Location: See all (5) locations...
Study Type: Observational
SUMMARY
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• 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
Locations
Other Locations
Switzerland
Universitätsspital Basel
RECRUITING
Basel
Insel Gruppe AG, Inselspital Bern
RECRUITING
Bern
Luzerner Kantonsspital
RECRUITING
Lucerne
Kantonsspital Winterthur
RECRUITING
Winterthur
Stadtspital Treimli
RECRUITING
Zurich
Contact Information
Primary
Lukas C Hunziker Munsch, Prof MD
lukas.hunziker@insel.ch
0041316322111
Backup
Monika Fürholz, MD
monika.fuerholz@insel.ch
00413163221 11
Time Frame
Start Date: 2019-08-09
Estimated Completion Date: 2034-08-31
Participants
Target number of participants: 1500
Related Therapeutic Areas
Sponsors
Leads: Insel Gruppe AG, University Hospital Bern