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Clinical Trials in China / NCT04012671
Recruiting Observational

A Registered Cohort Study on Duchenne Muscular Dystrophy

NCT04012671 · tracked via the Priya Life Science China tracker
Sponsor
Ning Wang, MD., PhD.
Phase
Observational
Started
2019-07-01
Last updated
2021-03-22

Condition(s) studied

Duchenne Muscular Dystrophy

Study summary

Dystrophinopathy is a term of X-linked recessive genetic disease, including Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and the X-linked dilated cardiomyopathy. The aim of this study is to determine the clinical spectrum and natural progression of dystrophinopathy in a prospective multicenter natural history study, to assess the clinical, genetic of patients with dystrophinopathy to optimize clinical management.

Eligibility

Sex
ALL
Min age
2 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Beyond 2 years old * Diagnosis with Duchenne Muscular Dystrophy, and female carriers, genotypically confirmed * Diagnosis should be supported by muscle biopsy, if no genetic confirmation. Exclusion Criteria: * Presence of other clinically significant illness

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
First Affiliated Hospital of Fujian Medical University Fuzhou China Recruiting

More Ning Wang, MD., PhD. trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04012671 on ClinicalTrials.gov ↗ ← All trials in China