Ultrafast ultrasound biomarkers to track Duchenne and Becker muscular dystrophy
Official title: Multiparametric Ultrafast Ultrasound Evaluation of Skeletal Muscle in Duchenne and Becker Muscular Dystrophies
Run by Nantes University Hospital · NCT07378553 · Data updated 2026-11-12
This study tests whether multiparametric ultrafast ultrasound can non-invasively monitor disease progression in people with Duchenne or Becker muscular dystrophy.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 5 Years to 60 Years |
| Sex | Men only |
| Enrollment | 60 (estimated) |
| Sponsor | Nantes University Hospital Academic / other |
| Locations | 1 site (Nantes) |
| Status | Recruiting |
| Started | March 3, 2026 |
| Main results expected | March 3, 2029 |
| Study ends | March 3, 2029 |
| Registry record updated | June 24, 2026 |
| Trial ID | NCT07378553 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are ambulatory or non-ambulatory males aged 5–60 with genetically confirmed Duchenne or Becker muscular dystrophy.
✕Probably not a fit
Patients with conditions preventing ultrasound assessment or inability to consent may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Researchers will compare muscle ultrasound measurements in ambulatory and non-ambulatory males with Duchenne or Becker muscular dystrophy to those of healthy age-matched peers over 12 months. The ultrafast ultrasound method simultaneously assesses muscle structure, mechanics, and physiology, including stiffness, anisotropy, viscosity, fat content, volume, and microvascular flow. The goal is to identify objective, sensitive markers of disease progression that could serve as outcome measures in future trials. The study will relate imaging-derived muscle changes to everyday functional performance such as walking and strength.
Why it matters
Potential benefit: If successful, this approach could provide a non-invasive, objective way to track disease progression and response to therapies in DMD/BMD.
How similar studies have gone: Previous research suggests ultrasound-based biomarkers can reflect muscle changes, but this multiparametric ultrafast approach is novel for DMD/BMD.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Inclusion Criteria for patients with Duchenne Muscular Dystrophy: Ambulatory and non-ambulatory males (ages 5-30 at baseline testing) previously diagnosed with Duchenne Muscular Dystrophy based on absence of dystrophin expression. * Inclusion Criteria for patients with Becker Muscular Dystrophy: Ambulatory and non-ambulatory males (ages 5-60 at baseline testing) previously diagnosed with Becker Muscular Dystrophy based on genetically confirmed, reduced or dysfunctional dystrophin. * Inclusion Criteria for Aged-matched controls: Ambulatory males (ages 5-60 years) without disease or injury to the lower and/or upper extremities Exclusion Criteria: * Exclusion Criteria for patients with Duchenne and Becker Muscular Dystrophies: Inability to undergo static exam, missing measurement site (resection/amputation), neurocognitive impairment preventing informed consent * Exclusion Criteria for Age-matched controls: Any condition affecting muscle metabolism/function, neuromuscular disease, or injury to the lower and/or upper extremities in the past 5 years
Where it's running
-
CHU de Nantes
Nantes, France Recruiting
Study contacts
- Study coordinator: Yann PEREON
- Email: yann.pereon@chu-nantes.fr
- Phone: 0240083704
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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GNT0004 gene therapy for Duchenne muscular dystrophy in ambulant boys
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AOC 1044 in Duchenne Muscular Dystrophy with Exon 44 Skipping
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DMD gene changes and heart function in boys and young men with dystrophinopathies
This study will test whether specific DMD gene changes and routine heart tests (blood biomarkers, ECG, and echocardiography) can help identify early heart problems in boys and young men aged 2–24 with genetically confirmed dystrophinopathies.
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Duchenne/Becker Muscular Dystrophy Registry for patients and carriers
This registry tests whether patients with Duchenne or Becker muscular dystrophy, or symptomatic female carriers, can be enrolled and followed across specialist centers to improve data sharing and care.
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.