Evaluating VM100 Nutritional Supplement for Improving Quality of Life in Duchenne Muscular Dystrophy Patients
Part of paid clinical trials in Gainesville, Florida.
- Sponsor
- University of Florida
- Study ID
- NCT07766980
- Status
- Recruiting
Conditions
- DMD
- Duchenne Disease
- Duchenne Muscular Dystrophy
- Muscular Dystrophy
- Muscular Dystrophy in Children
Eligibility Criteria
- Sex
- MALE
- Age
- 6 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- VM100 Nutritional Supplement — DIETARY_SUPPLEMENTVM100 is an investigational dietary supplement formulated specifically for individuals with Duchenne muscular dystrophy. It contains ten naturally derived ingredients formulated using a proprietary technology to enhance bioavailability. The supplement is intended to support mitochondrial function, reduce inflammation and oxidative stress, improve cognitive function and mood, and promote overall quality of life. Participants will self-administer the supplement orally twice daily during the intervention period.
Study Details
This pilot study will investigate the potential efficacy of VM100, a nutritional supplement specifically formulated for patients with DMD, on quality of life and physical symptoms. Twenty patients (aged 8 an over) will be enrolled to undergo a 10-week placebo-controlled intervention with VM100. Outcomes will include validated questionnaires and qualitative interview to assess impact on mental, cognitive and mood related measures, as well as endurance and fatigue).
Key Dates
- First listed
- Aug 17, 2026
- Start date
- Jul 27, 2026
- Status verified
- Oct 2025
- Primary completion
- Dec 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: VM100 Nutritional SupplementParticipants will receive the VM100 nutritional supplement orally twice daily for 10 weeks, consisting of 6 weeks of supplementation, followed by a 2-week washout period without supplementation, and a final 2 weeks of supplementation.
Primary Outcome Measure
Changes in DMD Quality of Life Physical Symptoms Domain Score [ Time Frame: Baseline, Weeks 2, 6, 8, and 10 ]
Central Contacts
- Tanja Taivassalo(352) 294 - 8748
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Florida | Gainesville | Florida | 32610 | Tanja Taivassalo (PRINCIPAL_INVESTIGATOR) |
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