CompletedNot applicableNCT02746718
Frequency of Pompe's Disease and Neuromuscular Etiologies in Patients With Restrictive Respiratory Failure Associated With Signs of Muscle Weakness
Studying Glycogen storage disease due to acid maltase deficiency
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
- Centre Hospitalier Universitaire de Nice
- Principal Investigator
- Sabrina SacconiCentre Hospitalier Universitaire de Nice
- Intervention
- Blood sample(other)
- Enrollment
- 50 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2015 – 2019
Study locations (21)
- CHU d'Angers, Angers, France
- Centre hospitalier d'Argenteuil, Argenteuil, France
- CHU de Brest, Brest, France
- CH d'Escartons, Briançon, France
- CH de Cannes, Cannes, France
- CHI de Créteil, Créteil, France
- CHU le Bocage, Dijon, France
- CHRU de Lille, Lille, France
- CHU de Limoges, Limoges, France
- Cabinet Dr Pereira-Cortese, Nice, France
- CHU de Nice, Nice, France
- GH Pitié Salpêtrière, Paris, France
- Hôpital Raymond Poincaré, Paris, France
- Hôpital Saint Louis, Paris, France
- Hôpital Tenon, Paris, France
- +6 more locations on ClinicalTrials.gov
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 NCT02746718 on ClinicalTrials.govOther trials for Glycogen storage disease due to acid maltase deficiency
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