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Study identifier: NCT05019625 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Biomarker Development for Muscular Dystrophies

Condition: Myotonic Dystrophy · Duchenne Muscular Dystrophy · Becker Muscular Dystrophy  ·  Sponsor: Massachusetts General Hospital

PhaseN/A
Planned participants465
Who can joinAll sexes, 5 Years to no upper limit
Healthy volunteersYes

About this study

Current methods of measuring the response to new treatments for muscular dystrophies involve the examination of small pieces of muscle tissue called biopsies. The investigators are interested in finding less invasive methods that reduce the need for muscle biopsies. The purpose of this research is to learn about the possibility of detecting and measuring the activity and severity of muscular dystrophies by examining a urine sample and a blood sample, and some muscles in the arms and legs using tests called ultrasound and electrical impedance myography; both tests are painless and non-invasive. The information that is gathered from this study may help to evaluate, prevent, diagnose, treat, and improve the understanding of human muscle diseases.

This description comes directly from the study's public registry record.

Talk to the study team

Tamkin Shahraki, MD  ·  617-726-7506  ·  tshahraki@mgh.harvard.edu

Always discuss trial participation with your own doctor first.

Locations (5)

Boston Children's HospitalBoston, Massachusetts, United StatesActive Not Recruiting
Brigham and Women's HospitalBoston, Massachusetts, United StatesRecruiting
Massachusetts General HospitalBoston, Massachusetts, United StatesRecruiting
Wake Forest UniversityWinston-Salem, North Carolina, United StatesRecruiting
University of PittsburghPittsburgh, Pennsylvania, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05019625