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Duchenne Muscular Dystrophy (DMD)NCT07674758

Modeling Mortality in Duchenne Muscular Dystrophy Cardiomyopathy: Identification of Surrogate Outcome Measures for DMD Drug Trials

An observational study of Duchenne Muscular Dystrophy (DMD) and Cardiomyopathy, run by Vanderbilt University Medical Center at 9 sites in United States.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

Dystrophin associated heart dysfunction is a leading cause of death in patients with Duchenne and Becker Muscular dystrophy (DMD/BMD) and Duchenne and Becker muscular dystrophy carriers (MDC); however, the evolution of heart dysfunction is not well-understood. Read more about this study

Who is it for?
Any age
How many people
1,000 participants
Where
9 sitesUnited States
Study dates
6 Jan 2025to 1 Feb 2029
How long will I take part?
5 Years
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Clinical phenotype of Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or muscular dystrophy carrier (MDC) confirmed with muscle biopsy or genotype

Who may be able to join

  • Clinical phenotype of Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD), or muscular dystrophy carrier (MDC) confirmed with muscle biopsy or genotype

Who cannot join

  • Additional genetic or congenital abnormality that may affect cardiovascular function or progression
  • Current investigational therapy that may affect cardiovascular function (would preclude ongoing data collection but prior data would still be used)

Trial locations and contacts

9 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Jonathan Soslow, MD, MSCI contact

615-322-7447

DMDMachineLearning@vumc.org

9 sites in 1 country

United States9 sites, 9 recruiting
  • Lurie Children's

    Chicago, Illinois, 60611

    Study Coordinator, 312-227-4100

    Recruiting
  • Nationwide Children's

    Columbus, Ohio, 43205

    Study Coordinator, 614-722-2555, DMDmachinglearning@vumc.org

    Recruiting
  • Duke Children's Hospital

    Durham, North Carolina, 27705

    Study Coordinator, 919-668-4000, DMDmachinelearning@vumc.org

    Recruiting
  • Riley Children's Hospital

    Indianapolis, Indiana, 46202

    Study Coordinator, 317-944-8906, DMDMachineLearning@vumc.org

    Recruiting
  • Vanderbilt University Medical Center

    Nashville, Tennessee, 37232

    Study Coordinator, 615-322-7447, DMDMachineLearning@vumc.org

    Recruiting
  • Children's Hospital of Richmond at VCU

    Richmond, Virginia, 23220

    Study Coordinator, (804) 828-2467, DMDmachinelearning@vumc.org

    Recruiting
  • UC Davis

    Sacramento, California, 95616

    Study Coordinator, 916-734-3456, DMDmachinelearning@vumc.org

    Recruiting
  • Seattle Children's

    Seattle, Washington, 98105

    Study Coordinator, 206-987-2515, DMDmachinelearning@vumc.org

    Recruiting
  • Children's National

    Washington D.C., District of Columbia, 20010

    Study Coordinator, 202-476-2090, DMDmachinelearning@vumc.org

    Recruiting

Other trials in United States

About this study

Official title: Evaluating Cardiac Function in Patients With Duchenne Muscular Dystrophy

Dystrophin associated heart dysfunction is a leading cause of death in patients with Duchenne and Becker Muscular dystrophy (DMD/BMD) and Duchenne and Becker muscular dystrophy carriers (MDC); however, the evolution of heart dysfunction is not well-understood. The central objectives of this proposal are to elucidate this evolution of heart dysfunction and identify measures from cardiac MRI images that can predict death or significant heart disease in patients with DMD/BMD/MDC. This study will create a large clinical and cardiac MRI registry of dystrophin associated heart dysfunction, will utilize advanced image analysis techniques, including deep learning neural networks, to comprehensively evaluate every patient, and will create a risk toolkit accessible to clinicians around the world; this proposal has the potential to improve the quality of life in patients with dystrophin associated heart dysfunction by allowing for earlier and more intensive therapy in patients with severe disease and by identifying surrogate outcome measures for use in therapeutic trials.

Read the detailed description

Duchenne and Becker muscular dystrophy (DMD/BMD) are devastating diseases with no cure resulting in loss of ambulation, respiratory failure, cardiomyopathy, and premature death. Dystrophin associated cardiomyopathy (defined here as CM) is the leading cause of death in DMD/BMD, and an under-studied concern in DMD and BMD mutation carriers (MDC). CM progression is variable and poorly described in the current era. There are no blood or imaging biomarkers that can predict the pace of progression or the risk of early mortality. More importantly, there are no established cardiac outcome measures. Novel, targeted therapeutics are necessary to treat CM, but these significant knowledge gaps make clinical trials challenging. A better understanding of DMD/BMD/MDC cardiovascular disease progression and the identification of surrogate outcome measures are critical for the field to advance. To address these obstacles, the investigators propose to leverage the Duchenne muscular dystrophy cardiac care consortium (DMDCCC). Created with grants from the NHLBI and the FDA, this consortium consists of twelve high-volume sites with similar DMD/BMD/MDC cardiovascular treatment and diagnostic protocols, including surveillance CMR imaging every 1-2 years. This proposal will create a comprehensive prospective registry of DMD/BMD/MDC patients with meticulously collected clinical data and cardiac magnetic resonance (CMR) images; we anticipate enrollment of 950 patients with over 4000 CMR studies. This cohort will be used to better define the progression of CM and to determine associations with mortality. The central hypothesis of this proposal is that integrated statistical modeling based on advanced imaging can improve prediction of CM progression and mortality. Aim 1 will create a comprehensive cohort of DMD/BMD/MDC patients and model the progression of CM. Aim 2 will determine cardiovascular measures that are associated with CM mortality or rapid progression using novel, data-driven, personalized machine learning models. Aim 3 will create a portal for DMD/BMD/MDC centers to determine patient risk. This multi-PI proposal leverages expertise in clinical care, cardiac imaging, biomedical engineering, complex image analysis, and neural networks. This study will create the largest cohort of DMD/BMD/MDC patients with CMR images, allowing for a better understanding of CM progression and identifying biomarkers that associate with poor outcomes. The resulting risk portal will provide clinicians all over the world with a method to assess their patient's risk in real time, allowing intensification of therapy for those deemed high risk. By building on prior productive collaborations, particularly that of the DMDCCC, this proposal will expand our understanding of CM, improving clinical care and future cardiac-specific therapeutic trials.

Keywords
Duchenne Muscular Dystrophy, cardiomyopathy, machine learning, cardiac MRI, Biomarker, Outcome measures
Medical subject headings
Muscular Dystrophy, Duchenne, Cardiomyopathies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07674758
Study groupRoleWhat they receive
Duchenne Muscular Dystrophy, Becker muscular dystrophy, and carriers of muscular dystrophyEvaluation of surrogate outcome measures of disease in patients with dystrophinopathy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Mortality

    Time from biomarker of interest to mortality

    Measured: baseline to 10 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Jun 2026
  2. Study start6 Jan 2025
  3. Primary completion1 Feb 2029 (estimated)
  4. Study completion1 Feb 2029 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
1,000 participants (estimated)
Target duration
5 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07674758
Sponsor's protocol ID
240203
Other IDs
R01HL167969
Status last verified
Jul 2026
First submitted
24 Jun 2026
Last updated
28 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: The data will be shared with C-PATH

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