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Evaluation of Predictive Factors for Right Ventriculaire Dysfunction

NCT04596982 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 18

Last updated 2025-08-22

No results posted yet for this study

Summary

An observational study of patients in cardiogenic shock under veno-arterial ECMO is designed to describe the clinical, ultrasound and hemodynamic parameters of these patients and to establish a predictive score for right-sided dysfunction in a patient within 48 hours of ECMO withdrawal after placement of IMPELLA®.

Conditions

  • Right Ventriculaire Dysfunction

Interventions

OTHER

Placement of IMPELLA®

ultrasound and hemodynamic parameters of patients in order to establish a predictive score for right-sided dysfunction after placement of IMPELLA®

Sponsors & Collaborators

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-04-09
Primary Completion
2023-10-25
Completion
2023-10-25

Countries

  • France

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 NCT04596982 on ClinicalTrials.gov