TerminatedPhase 3NCT00927732
Hydroquinidine Versus Placebo in Patients With Brugada Syndrome
Studying Brugada 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
- Nantes University Hospital
- Principal Investigator
- V Probst, PrCHU NANTES - Hôpital Laennec
- Intervention
- hydroquinidine(drug)
- Enrollment
- 64 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2009 – 2014
Study locations (17)
- CHU Amiens, Amiens, France
- CHU Angers, Angers, France
- CHU Bordeaux, Bordeaux, France
- CHU Brest, Brest, France
- CHU Grenoble, Grenoble, France
- CHRU Lille, Lille, France
- CHU Lyon, Lyon, France
- AP-HM Marseille, Marseille, France
- CHU Montpellier, Montpellier, France
- CHU Nancy, Nancy, France
- CHU Nantes, Nantes, France
- AP-HP Paris Lariboisière, Paris, France
- CHU Poitiers, Poitiers, France
- CHU Rennes, Rennes, France
- CHU Strasbourg, Strasbourg, France
- +2 more locations on ClinicalTrials.gov
Collaborators
Sanofi
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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