CompletedPhase 3NCT04113187
Propranolol for Epistaxis in Hereditary Hemorrhagic Telangiectasia Patients
Studying Hereditary hemorrhagic telangiectasia
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
- University Hospital, Bordeaux
- Principal Investigator
- Anne CONTIS, MDUniversity Hospital, Bordeaux
- Intervention
- Propranolol treatment(drug)
- Enrollment
- 15 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2022
Study locations (1)
- CHU de Bordeaux - service de médecine interne, Bordeaux, France
Collaborators
AMRO-HHT-France - Association Maladie de Rendu-Osler
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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