Actively Recruiting

Age: 18Years +
All Genders
ID07334457

Study of Platelet Population Changes Under Circulatory Support With ECMO

Led by University Hospital, Strasbourg, France · Updated on 2026-01-12

75

Participants Needed

1

Research Sites

1 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how different types of blood platelets change in adults receiving extracorporeal membrane oxygenation (ECMO) support, which is used for severe cardiac or respiratory failure. Advances in flow cytometry have shown four major platelet types with different functions, and changes in these types may relate to complications during ECMO treatment. This observational study aims to better understand these platelet population changes over time under ECMO support. The study observes adult patients treated with veno-arterial or veno-venous ECMO implanted within the previous 24 hours in intensive care units. There are no investigational treatments or interventions being administered; instead, platelet populations are monitored at specific time points after ECMO initiation, specifically on days 1, 3, and 7. This approach helps researchers document how platelet types shift during the first week of ECMO therapy. Participants will be involved in blood sample collections to assess platelet populations at the defined days after ECMO starts. These assessments involve flow cytometry techniques to measure the proportions of native, proaggregating, procoagulant, and apoptotic platelets. The primary outcome focuses on these proportional changes. The study is sponsored by University Hospital, Strasbourg, and participation lasts for the week following ECMO initiation, with no additional treatments provided as part of the study.

CONDITIONS

Brief Title

Study of Platelet Population Changes Under Circulatory Support With ECMO

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient (≥18 years) treated in one of the intensive care units of the Anesthesia and Intensive Care Department at Strasbourg University Hospital.
  • Implanted with veno-arterial or veno-venous ECMO within the previous 24 hours.
Not Eligible

You will not qualify if you...

  • Subject who has expressed their opposition to participating in the study.
  • Subject under legal protection.
  • Subject under guardianship or curatorship.

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 7 days

Participants are observed while receiving ECMO treatment to assess changes in platelet populations.

3 visits on Days 1, 3, and 7 after the initiation of ECMO treatment

Trial Site Locations

Total: 1 location

1

Service d'anesthésie-réanimation - CHU de Strasbourg - France

Strasbourg, France, 67091

Actively Recruiting

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Research Team

C

Charles TACQUARD, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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