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NCT05989620Recruiting

Long-Term Development of Muscular Dystrophy Outcome Assessments

Long-Term Development of Muscular Dystrophy Outcome Assessments (GRASP-01-005)

Source: ClinicalTrials.gov · Last updated 18 Nov 2025

Brief summary (registry, in English)

This is a 24-month, observational study of up to 1000 participants with Limb Girdle Muscular Dystrophy (LGMD), Myotonic Dystrophy Type 2 (DM2), and late onset Pompe disease (LOPD).

Status (registry)
Recruiting
Study type
Observational
Enrollment
1000 (estimated)
First submitted
2 Aug 2023
Start date
18 Oct 2023
Primary completion date
1 Oct 2028
Lead sponsor
Virginia Commonwealth University
NCT number
NCT05989620

What you commit to

  • Study type: Observational
  • Planned participants: 1000
  • From 18 Oct 2023 to the primary completion date, 1 Oct 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation in a clinical trial receiving an investigational product

Other illness

  • Any other illness that would interfere with the ability to undergo safe testing or would interfere with interpretation of the results in the opinion of the site investigator

Who the study is looking for

  • Age between 6-50 years at enrollment
  • Clinically affected (defined as weakness on bedside evaluation in a pattern consistent with proximal weakness)
  • Genetic confirmation of a LGMD, DM2, or LOPD
  • FVC above 30% of predicted

Age in the registry: 6 years to 50 years · Sex: All

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Virginia Commonwealth University
Coordinator of this site? Confirm its status
RichmondUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.