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CARDSUP - SWISS Circulatory Support Registry — CARDSUP  

Cardiogenic Shock Clinical Trial

Official title:
Clinical Outcomes in Patients in Need of a Non-permanent Extracorporeal Cardiocirculatory Support System (Peripheral Extracorporeal Membrane Oxygenation (ECMO) or Axial Flow Pump IMPELLA)

Clinical Trial 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.

Clinical Trial Description

This prospective data collection is made up of an all-comers design, including all eligible consecutive patients receiving an Impella (2.5, 5, CP, or RP) or VA-ECMO device via femoral access who gave their consent (or, if not possible, their relative). 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04117230
Study type Observational [Patient Registry]
Source Insel Gruppe AG, University Hospital Bern
Contact Lukas C Hunziker Munsch, PD
Phone 0041316322111
Email lukas.hunziker@insel.ch
Status Recruiting
Phase
Start date August 9, 2019
Completion date August 31, 2034
View Details
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