RecruitingNCT03773159
Development of a Device for Evaluating Primary Hemostasis Under Whole Blood Flow Conditions
Studying Von Willebrand disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Centre Hospitalier Universitaire Dijon
- Intervention
- Blood sampling(biological)
- Enrollment
- 200 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2026
Study locations (2)
- CHU de Besançon, Besançon, France
- CHU Dijon Bourgogne, Dijon, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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