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CARDSUP - SWISS Circulatory Support Registry

NCT04117230 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1500

Last updated 2024-12-06

No results posted yet for this study

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.

Conditions

  • Cardiogenic Shock

Sponsors & Collaborators

  • Insel Gruppe AG, University Hospital Bern

    lead OTHER

Principal Investigators

  • Lukas C Hunziker Munsch, Prof MD · University of Bern

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-08-09
Primary Completion
2034-08-31
Completion
2034-08-31

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04117230 on ClinicalTrials.gov