CompletedNCT03157154
Bleeding Risk Evaluation in Haemophilia Patients Under Antiplatelet Therapies
Studying Hemophilia
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
- Nantes University Hospital
- Principal Investigator
- Marc Trossaërt, DrNantes University Hospital
- Intervention
- Non interventional study(other)
- Enrollment
- 259 enrolled
- Eligibility
- 50 years · MALE
- Timeline
- 2017 – 2017
Study locations (6)
- Angers University Hospital, Angers, France
- Brest University Hospital, Brest, France
- Le Mans Hospital, La Mans, France
- Lyon University Hospital, Lyon, France
- Rennes University Hospital, Rennes, France
- Tours University Hospital, Tours, 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.
Open NCT03157154 on ClinicalTrials.govOther trials for Hemophilia
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