Collection of samples from patients with neuromuscular diseases
Official title: Center for Inherited Muscle Research Neuromuscular Research Biobank
Run by Virginia Commonwealth University · NCT05434572 · Data updated 2026-11-12
This study is collecting blood, skin, and muscle samples from people with neuromuscular diseases to help researchers learn more about these conditions in the future.
Quick facts
| Study type | Observational |
|---|---|
| Ages | Any age to 75 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Virginia Commonwealth University Academic / other |
| Locations | 1 site (Richmond, Virginia) |
| Status | Recruiting |
| Started | March 17, 2021 |
| Main results expected | January 2030 |
| Study ends | February 2030 |
| Registry record updated | July 6, 2026 |
| Trial ID | NCT05434572 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include individuals with a diagnosed or suspected neuromuscular disease, those with a family history of such diseases, or healthy volunteers aged from neonates to 75 years.
✕Probably not a fit
Patients who are unwilling to provide informed consent will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This research repository aims to collect, store, and share biological samples from individuals diagnosed with various neuromuscular diseases. Participants will provide medical information and biological samples such as blood, skin cells, and muscle tissue, which will be stored at Virginia Commonwealth University for future research. The study emphasizes informed consent, ensuring participants understand the process and can ask questions before contributing samples. The collected data will facilitate further research into neuromuscular disorders.
Why it matters
Potential benefit: If successful, this biobank could enhance understanding and treatment options for neuromuscular diseases.
How similar studies have gone: While biobanks for neuromuscular diseases are not novel, the success of similar repositories has shown promise in advancing research in this field.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Willing and able to give informed consent * Positive diagnosis or suspected diagnosis of neuromuscular disease, or * Family history of neuromuscular disease, or * Healthy volunteer * Age Neonates-75 Exclusion Criteria: * Unwilling to sign consent
Where it's running
-
Virginia Commonwealth University
Richmond, Virginia, United States Recruiting
Study contacts
- Principal investigator: Nicholas E. Johnson, MD — Virginia Commonwealth University
- Study coordinator: Nicholas Johnson
- Email: nicholas.johnson@vcuhealth.org
- Phone: 804-628-1624
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Gamified 6-Minute Walk Test for Children with Neuromuscular Disorders
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Evaluating respiratory functions and exercise capacity in children with neuromuscular diseases
This study is trying to see how well children with Duchenne Muscular Dystrophy and Spinal Muscular Atrophy can breathe and exercise compared to healthy kids.
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Research network for hereditary spastic paraplegia and primary lateral sclerosis
This study is trying to learn more about hereditary spastic paraplegia and primary lateral sclerosis by enrolling people with specific types of the condition to help find better treatments and understand how these diseases progress.
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This study is testing new technology to see how well it can track and understand limb movements in people with neuromuscular diseases compared to those without any movement issues.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.