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Study of Platelet Population Changes Under Circulatory Support With ECMO

Study of Platelet Population Changes Under Circulatory Support With ECMO

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07334457
Acronym
ECMO-POP
Enrollment
75
Registered
2026-01-12
Start date
2025-03-11
Completion date
2027-03-11
Last updated
2026-01-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cardiac Failure, Respiratory Failure

Keywords

Cardiac Failure, Respiratory Failure

Brief summary

Advances in flow cytometry techniques have led to a better understanding of platelet phenotypes and have revealed the existence of four major platelet populations with distinct functional properties (native, proaggregating, procoagulating, or apoptotic). These phenotypes have a significant impact on the hemostatic capacity of blood platelets, and a proportional change in these populations during ECMO treatment could, at least in part, contribute to the observed complications.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* 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.

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Proportional Changes in the Different Platelet Populations (native, proaggregating, procoagulant, or apoptotic)Days 1, 3, and 7 after the initiation of ECMO treatment.Proportional Changes in the Different Platelet Populations (native, proaggregating, procoagulant, or apoptotic) on Days 1, 3, and 7 after the initiation of ECMO treatment.

Countries

France

Contacts

Primary ContactCharles TACQUARD, MD, PhD
charlesambroise.tacquard@chru-strasbourg.fr33.3.69.55.16.08

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026