Not yet recruitingNCT06884384
DOAC Versus VKA in Patients With Non-high-risk APS : Prospective Cohort Study
Studying Antiphospholipid syndrome
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
- Central Hospital, Nancy, France
- Principal Investigator
- Virginie DUFROST, MDCHRU - Nancy
- Intervention
- Additional blood collection during routine blood sampling at the inclusion (33.9 ml) and at the thrombotic recurrence (between 3.5 and 5 ml)(biological)
- Enrollment
- 310 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2031
Study locations (13)
- Central Hospital, Nancy, France, Vandœuvre-lès-Nancy, Grand Est, France
- CHU d'Amiens, Amiens, France
- CHU de Besançon, Besançon, France
- CHU de Brest, Brest, France
- CHU de Dijon, Dijon, France
- CHU de Lyon, Lyon, France
- Hôpital Robert Schuman, UNEOS, Metz, France
- CH de Mulhouse, Mulhouse, France
- CHU de Nantes, Nantes, France
- Hôpital Lariboisière - APHP, Paris, France
- CHU de Reims, Reims, France
- CHU de Saint Etienne, Saint-Priest-en-Jarez, France
- CHU de Strasbourg - Hôpital civil, Strasbourg, 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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