Longitudinal Study of the Natural History of Duchenne Muscular Dystrophy (DMD)
NCT00468832 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 551
Last updated 2016-04-21
Summary
The purpose of this study is to establish the largest long-term assessment of people with Duchenne muscular dystrophy (DMD). In this study, the investigators associated with the Cooperative International Neuromuscular Research Group CINRG) will take a detailed look (for a minimum of eight years) at DMD participant's physical abilities, the medical problems they experience, and how they use health care services. Physical abilities will be compared to a group of healthy controls.
The second purpose of this study is to find out whether small, normal differences in the genetic makeup of people with DMD (called "single nucleotide polymorphisms" or "SNPs") affect how their disease progresses and relates to muscle strength/size and steroid response.
The third purpose of this study is to study genetic variations associated with DMD.
The final purpose of this study is to determine whether certain biomarkers are present in people with DMD and not in healthy controls.
Conditions
Sponsors & Collaborators
-
U.S. Department of Education
collaborator FED -
National Institutes of Health (NIH)
collaborator NIH -
United States Department of Defense
collaborator FED -
Parent Project Muscular Dystrophy
collaborator OTHER -
Cooperative International Neuromuscular Research Group
lead NETWORK
Principal Investigators
-
Craig McDonald, MD · University of California, Davis
Eligibility
- Min Age
- 2 Years
- Max Age
- 30 Years
- Sex
- MALE
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2005-12-31
- Primary Completion
- 2019-12-31
- Completion
- 2019-12-31
Countries
- United States
- Argentina
- Australia
- Canada
- India
- Israel
- Italy
- Sweden
Study Locations
More Related Trials
-
The Burden of Access in Duchenne Muscular Dystrophy in the US
NCT03951675 ·Status: COMPLETED
-
The Baby Duchenne Study: Characterizing Developmental and Clinical Outcomes in the First Three Years in Children With Duchenne Muscular Dystrophy
NCT07092540 ·Status: RECRUITING
-
Comprehensive Study of Duchenne Muscular Dystrophy at Sohag University Hospital
NCT05029232 ·Status: UNKNOWN ·Phase: NA
-
A Natural History Study In Chinese Male Patients With Duchenne Muscular Dystrophy
NCT03760029 ·Status: COMPLETED ·Phase: NA
-
Strength Training in Duchenne Muscular Dystrophy
NCT02421523 ·Status: COMPLETED ·Phase: NA
-
Natural History Study of Patients With Limb-Girdle Muscular Dystrophy 2I
NCT03842878 ·Status: COMPLETED
-
Development of a Registry to Assess Natural History in Duchenne Muscular Dystrophy
NCT06579859 ·Status: NOT_YET_RECRUITING
-
Prognostic Factors Affecting Duchenne Muscular Dystrophy
NCT03372655 ·Status: UNKNOWN
-
Study of Genotype and Phenotype Characterization in Duchenne Muscular Dystrophy With Small Mutations
NCT05833633 ·Status: UNKNOWN
-
phenotypeS in Non Ambulant Duchenne Muscular Dystrophy
NCT06366815 ·Status: RECRUITING
-
Endomysial Fibrosis, Muscular Inflammatory Response and Calcium Homeostasis Dysfunction in Duchenne Muscular Dystrophy
NCT01823783 ·Status: UNKNOWN ·Phase: NA
-
Long-Term Development of Muscular Dystrophy Outcome Assessments
NCT05989620 ·Status: RECRUITING
-
Assessment of Cardiopulmonary Function in Duchenne Muscular Dystrophy
NCT02195999 ·Status: COMPLETED
-
Improved Muscle Function in Duchenne Muscular Dystrophy Through L-Arginine and Metformin
NCT02516085 ·Status: COMPLETED ·Phase: PHASE1
-
Molecular Analysis of Patients With Neuromuscular Disease
NCT00390104 ·Status: RECRUITING
-
Non-invasive Imaging of Muscle Structure in Duchenne Muscular Dystrophy Using Multispectral Optoacoustic Tomography
NCT03490214 ·Status: COMPLETED ·Phase: NA
-
Natural History of Duchenne Muscular Dystrophy
NCT03882827 ·Status: RECRUITING
-
This is a Study to Get More Information About Non Ambulatory Boys & Men With Duchenne Muscular Dystrophy
NCT01098708 ·Status: COMPLETED
-
Biomarker for Duchenne Muscular Dystrophy
NCT02994030 ·Status: COMPLETED
-
Multicenter Observational Study of Myotonic Dystrophy Type 1
NCT02308657 ·Status: COMPLETED
-
Magnetic Resonance Imaging and Biomarkers for Muscular Dystrophy
NCT01484678 ·Status: RECRUITING
-
Extracellular RNA Biomarkers of Duchenne Muscular Dystrophy
NCT05016908 ·Status: RECRUITING
-
Safety Study of Transvenous Limb Perfusion in Human Muscular Dystrophy
NCT00873782 ·Status: COMPLETED ·Phase: PHASE1
-
Safety and Efficacy Study of IGF-1 in Duchenne Muscular Dystrophy
NCT01207908 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Evaluation of Muscle miRNA as Biomarkers in Dystrophinopathies
NCT02109692 ·Status: UNKNOWN ·Phase: NA