New study maps key tests for LGMD to speed up drug development
NCT ID NCT03981289
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study involved 116 people with Limb Girdle Muscular Dystrophy (LGMD), a group of rare muscle-weakening disorders. Researchers measured how well participants could walk, move their arms, and breathe, and asked about their daily activities and overall health. The goal was to identify the best tests to track disease progression, which will help design future clinical trials for new treatments.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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John Walton Muscular Dystrophy Research Centre (Newcastle Upon Tyne)
Newcastle, United Kingdom
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Kennedy Krieger Institute
Baltimore, Maryland, 21205, United States
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Nationwide Children's Hospital
Columbus, Ohio, 43205, United States
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The University of Colorado Anschutz Medical Campus
Aurora, Colorado, 80045, United States
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University of California Irvine
Irvine, California, 92697, United States
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University of Iowa
Iowa City, Iowa, 52242, United States
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University of Kansas Medical Center
Kansas City, Kansas, 66160, United States
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University of Minnesota
Minneapolis, Minnesota, 55455, United States
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Virginia Commonwealth University
Richmond, Virginia, 23298, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can MRI scans reveal the hidden pattern of muscle damage in a rare muscular dystrophy?
- Virtual group therapy aims to boost social skills in kids with rare muscle disease
- Paving the way: new study aims to sharpen tools for LGMD R1 trials
- New study aims to sharpen tools for tracking becker muscular dystrophy
- New drug could help boys with duchenne walk and move longer