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Characterization of Clinical Skeletal and Cardiac Impairment in Carriers of Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD)
Longitudinal prospective observational study. This is a 24-month study with the possibility of extending the data time points. Initially baseline, then 12 and 24 months follow up studies will be completed.
Four cohorts are enrolled in this study. The target population is the cohort of genetically confirmed DMD/BMD female carriers (Cohort A). This cohort will consist of 150 DMD/BMD mothers who are somatic carriers of a mutation in the DMD gene. The data collected for this cohort will be compared to three control groups; Control Group B is a cohort of 50 DMD/BMD mothers who are NOT somatic carriers, Control Group C is a cohort of 50 age-matched healthy controls and Control Group D is a cohort of 25 genetically confirmed carriers who do not have an affected child. The inclusion of a Control Group B allows for a comparison to a group of mothers that share the emotional and cognitive burden of caring for an affected male without having the physical or cognitive risks of being a female carrier. The Control Group C offers robust data from an age-matched healthy cohort for purposes of comparison. Control Group D allows for comparison to a group of women that have the same physical or cognitive risks as the Cohort A female carriers, but do not have the same burden of care giving.
Age
18 - No limit years
Sex
FEMALE
Healthy Volunteers
Yes
Nationwide Children's Hosptial
Columbus, Ohio, United States
Start Date
June 1, 2016
Primary Completion Date
December 1, 2030
Completion Date
December 1, 2030
Last Updated
August 27, 2024
250
ESTIMATED participants
Genetic characterization
GENETIC
Lead Sponsor
Nationwide Children's Hospital
Collaborators
NCT07037862
NCT07160634
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06450639