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

Von Willebrand Diseases Clinical Trial

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

Clinical Trial Summary

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).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03773159
Study type Observational
Source Centre Hospitalier Universitaire Dijon
Contact Emmanuel De Maistre
Phone 03 81 61 56 15
Email emmanuel.demaistre@chu-dijon.fr
Status Recruiting
Phase
Start date May 6, 2019
Completion date May 2026
View Details
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