Impella in Cardiogenic Shock Registry
NCT06007963 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2023-08-23
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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