RECRUITINGOBSERVATIONAL
phenotypeS in Non Ambulant Duchenne Muscular Dystrophy
Characterizing Phenothypes in Non Ambulant Duchenne Muscular Dystrophy
About This Trial
The aims of the study are to prospectively collect information on several aspects of function in non-ambulant DMD patients by using a structured battery of tests including motor, respiratory and cardiac function
Who May Be Eligible (Plain English)
Who May Qualify:
- Children with genetically confirmed diagnosis of Duchenne Muscular Dystrophy will be included in the study. We will include all Duchenne Muscular Dystrophy boys who have lost the ability to walk independently.
- All patients in whom consent can be obtained will be enrolled with no exclusion criteria.
Who Should NOT Join This Trial:
- Patients lacking genetic confirmation of Duchenne Muscular Dystrophy
- Patients still able to walk for more than 10 meters.
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
Inclusion Criteria:
* Children with genetically confirmed diagnosis of Duchenne Muscular Dystrophy will be included in the study. We will include all Duchenne Muscular Dystrophy boys who have lost the ability to walk independently.
* All patients in whom consent can be obtained will be enrolled with no exclusion criteria.
Exclusion Criteria:
* Patients lacking genetic confirmation of Duchenne Muscular Dystrophy
* Patients still able to walk for more than 10 meters.
Treatments Being Tested
OTHER
Different Phenotypes of non ambulant patients with Duchenne Muscular Dystrophy
clinical and functional data collection of non ambulant patients with Duchenne muscular dystrophy
Locations (2)
IRCCS Eugenio Medea - Ass. "La Nostra Famiglia"
Bosisio Parini, Lc, Italy
Fondazione Policlinico Universitario A. Gemelli IRCCS
Roma, Italy