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Study identifier: NCT03773159 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Development of a Device for Evaluating Primary Hemostasis Under Whole Blood Flow Conditions

Condition: Von Willebrand Diseases · Major Constitutional Thrombopathy · Patient on Antiplatelet Drugs  ·  Sponsor: Centre Hospitalier Universitaire Dijon

PhaseN/A
Planned participants200
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

Currently, the exploration of primary hemostasis (a physiological phenomenon used to stop bleeding) is imperfect because it is based on targeted tests for platelets or von Willebrand factor, without taking into account blood flow and other blood cells (red and white blood cells). Tests for whole blood and flow conditions exist, but there is currently no test that comes close to actual physiological conditions. An exploration of whole blood haemostasis in a device that is similar to a blood vessel and at different flow conditions (venous and arterial) could help to better identify the risk of bleeding in predisposed patients (von Willebrand factor deficiency, antiplatelet therapy). The objective of the study is to evaluate the performance of this new hemostasis test in whole blood and under flow conditions. Participation in the study is ad hoc and is limited to adding a maximum of 4 citrated tubes (20 mL or the equivalent of 4 teaspoons) and 1 EDTA tube (5mL) to a routine blood sample (for patients) or during blood donation (for controls).

This description comes directly from the study's public registry record.

Talk to the study team

Emmanuel De Maistre  ·  03 81 61 56 15  ·  emmanuel.demaistre@chu-dijon.fr

Always discuss trial participation with your own doctor first.

Locations (2)

CHU de BesançonBesançon, FranceRecruiting
CHU Dijon BourgogneDijon, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT03773159