RecruitingPHASE2, PHASE3NCT05098704
Preventive Effect of Clopidogrel on the Systemic Sclerosis Development Risk
Studying Diffuse cutaneous systemic sclerosis
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
- Marie-Elise TRUCHETET, ProfUniversity Hospital, Bordeaux
- Intervention
- clopidogrel treatment(drug)
- Enrollment
- 90 enrolled
- Eligibility
- 18-85 years · All sexes
- Timeline
- 2022 – 2031
Study locations (10)
- CH de la Cote Basque - service de rhumatologie, Bayonne, France
- CHU de Bordeaux - service de Médecine Interne et Maladies Infectieuses, Bordeaux, France
- CHU de Bordeaux - service de rhumatologie, Bordeaux, France
- CHU de Brest - service de rhumatologie, Brest, France
- CHU de Grenoble Alpes - service de médecine vasculaire, Grenoble, France
- CH de Libourne - service de rhumatologie, Libourne, France
- CH de Mont-de-Marsan - service de rhumatologie, Mont-de-Marsan, France
- AP-HP - Hôpital Cochin - service de médecine interne, Paris, France
- CH de Pau - service de médecine interne, Pau, France
- CHU de Toulouse - service de médecine interne, Toulouse, France
Collaborators
Ministry for Health and Solidarity, 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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