Muscular Dystrophy, Duchenne Clinical Trial
— CPIOfficial title:
Assessment of Cardiopulmonary Function in Duchenne Muscular Dystrophy
NCT number | NCT02195999 |
Other study ID # | IRB201300420 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | December 2013 |
Est. completion date | March 6, 2019 |
Verified date | July 2019 |
Source | University of Florida |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This study seeks to develop and validate non-invasive assessments of cardiac and respiratory muscles with magnetic resonance imaging (MRI) to better predict the natural disease progression of Duchenne muscular dystrophy (DMD) in affected individuals over time, as well as determine whether peripheral skeletal muscle dysfunction can predict cardiopulmonary dysfunction. The central hypothesis is that non-invasive MRI measures of the heart, muscle, and peripheral skeletal muscles can sensitively predict future cardiopulmonary decline.
Status | Completed |
Enrollment | 9 |
Est. completion date | March 6, 2019 |
Est. primary completion date | March 6, 2019 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 5 Years to 15 Years |
Eligibility |
Inclusion Criteria: - Male - 5-15 years old at the time of enrollment - Diagnosed with DMD (as defined by parent project) - Written parental informed consent (and assent where appropriate) before any study procedures take place Exclusion Criteria: - Contraindication to an MRI examination - Presence of a secondary condition that impacts muscle function or metabolism, that leads to developmental delay or impaired motor control, or that is not stable - Participant is unable to comply with study requirements - Congenital structural abnormality of the heart, repaired or unrepaired - Clinically contraindicated participation |
Country | Name | City | State |
---|---|---|---|
United States | Clinical and Translational Research Building | Gainesville | Florida |
Lead Sponsor | Collaborator |
---|---|
University of Florida | CureDuchenne |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Magnetic Resonance (MRI) T2 and Magnetic Resonance Spectroscopy (MRS) | The MRI T2 and MRS will be used as a noninvasive marker of myocardial damage/inflammation of participants of this study as an early detection for DMD. | up to 4 years | |
Secondary | Pulmonary Function Testing (PFT) | Non-invasive breathing tests that characterize respiratory muscle function, as well as lung compliance and physiology. | up to 4 years | |
Secondary | Metabolic Exercise Testing (exercise capacity and MVO2) | With the use of metabolic exercise testing, the aim is to correlate changes in cardiopulmonary function with decline in peripheral skeletal muscle function in individuals with DMD. Metabolic exercise testing includes measuring exercise capacity and maximum oxygen consumption (MVO2). | up to 4 years | |
Secondary | Multiple-echo Dixon | The echocardiogram performed with the multiple-echo Dixon method helps to assess participants cross-sectionally and longitudinally for variations and changes in myocardial structure. This method and MRS will also be used for fat fraction determination. | up to 4 years |
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