Clinical trial Recruiting at 1 site Observational Ages 5 to 60 Men only

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.

More Becker Muscular Dystrophy trials

Quick facts

Study typeObservational
Ages5 Years to 60 Years
SexMen only
Enrollment60 (estimated)
SponsorNantes University Hospital
Academic / other
Locations1 site (Nantes)
StatusRecruiting
StartedMarch 3, 2026
Main results expectedMarch 3, 2029
Study endsMarch 3, 2029
Registry record updatedJune 24, 2026
Trial IDNCT07378553 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

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-15 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.