Decoding Central Defects in Dystrophinopathies From Diagnostic to Remediation
NCT07125898 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 110
Last updated 2025-08-15
Summary
The study aims to identify a genotype/phenotype correlation by analyzing more finely the neurodevelopmental disorders in DMD patients.
Conditions
- Dystrophinopathies
Sponsors & Collaborators
-
Assistance Publique - Hôpitaux de Paris
lead OTHER
Principal Investigators
-
Isabelle DESGUERRE, MD, PhD · Hôpital Universitaire Necker - Enfants Malades
Eligibility
- Min Age
- 5 Years
- Max Age
- 12 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-10-01
- Primary Completion
- 2027-10-01
- Completion
- 2029-04-01
Countries
- France
Study Locations
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