Impella in Cardiogenic Shock Registry

NCT06007963 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60

Last updated 2023-08-23

No results posted yet for this study

Summary

The purpose of the study is to evaluate the safety, efficacy and clinical usefulness of a mechanical support strategy with the impella device.

Conditions

  • Shock, Cardiogenic

Interventions

PROCEDURE

Treatment with impella device.

Impella percutaneous mechanical supported patients will be included after revision to support.

Sponsors & Collaborators

  • Universitaire Ziekenhuizen KU Leuven

    lead OTHER

Principal Investigators

  • Tom Adriaenssens, MD PhD · Universitaire Ziekenhuizen KU Leuven

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-29
Primary Completion
2024-01-01
Completion
2024-01-01

Countries

  • Belgium

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 NCT06007963 on ClinicalTrials.gov