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Study identifier: NCT06503367 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Observation Study in Patients Age 0-5 Years With LAMA2-related Congenital Muscular Dystrophy

Condition: LAMA2-MD \(Merosin Deficient Congenital Muscular Dystrophy, MDC1A\)  ·  Sponsor: Nationwide Children's Hospital

PhaseN/A
Planned participants44
Who can joinAll sexes, N/A to 5 Years
Healthy volunteersNo

About this study

The goal of this observational study is to understand how young children with LAMA2-related dystrophy move and change over time. We will also learn about how this condition impacts other body systems. Participants will undergo: * Neuromuscular assessments * Blood collections * Swallowing and breathing assessments * Questionnaires

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

Talk to the study team

Kevin Warf  ·  (614) 355-2765  ·  ReadyCMDLAMA2@nationwidechildrens.org

Always discuss trial participation with your own doctor first.

Locations (14)

University of California, Los AngelesLos Angeles, California, United StatesRecruiting
Stanford UniversityStanford, California, United StatesRecruiting
Ann & Robert H. Lurie Children's Hospital of ChicagoChicago, Illinois, United StatesRecruiting
University of Iowa Stead Family Children's HospitalIowa City, Iowa, United StatesRecruiting
National Institute of Neurological Disorders and Stroke, NIHBethesda, Maryland, United StatesRecruiting
Boston Children's HospitalBoston, Massachusetts, United StatesRecruiting
University of MinnesotaSaint Paul, Minnesota, United StatesRecruiting
Washington University in St. LouisSt Louis, Missouri, United StatesRecruiting
University of RochesterRochester, New York, United StatesRecruiting
Cincinnati Children's Hospital Medical CenterCincinnati, Ohio, United StatesRecruiting
Nationwide Children's HospitalColumbus, Ohio, United StatesRecruiting
Children's Hospital of PittsburghPittsburgh, Pennsylvania, United StatesRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06503367