CompletedNCT04043273
Treatment-related Benefit and Satisfaction in Fabry Patients. Insight in Patients Expectations and Preferences
Studying Fabry disease
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
- Amicus Therapeutics France SAS
- Principal Investigator
- Olivier Lidove, MDGroupe Hospitalier Diaconesses Croix Saint-Simon
- Intervention
- Noninterventional characterization of patients expectations and preferences regarding their treatment(behavioral)
- Enrollment
- 69 enrolled
- Eligibility
- 16 years · All sexes
- Timeline
- 2019 – 2023
Study locations (15)
- CHU d'Angers, Angers, France
- CHU Pellegrin, Bordeaux, France
- Hôpital Côte de Nacre, Caen, France
- CHU de Dijon, Dijon, France
- CHRU de Lille, Lille, France
- Hôpital Femme Mère Enfant, Lyon, France
- Hôpital de la Conception, Marseille, France
- CHU de Nantes, Nantes, France
- Hopital Tenon, Paris, France
- Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France
- CHU de Rennes, Rennes, France
- CHU de Rouen, Rouen, France
- CHU de Strasbourg, Strasbourg, France
- CHU de Toulouse, Toulouse, France
- CHU de Tours, 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.
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