Actively Recruiting
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
Eligibility Criteria
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.
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
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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