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Multimodal Brain Imaging Phenotypes and Genetic Associations in Duchenne Muscular Dystrophy

Multimodal Brain Imaging Phenotypes and Genetic Associations in Duchenne Muscular Dystrophy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500096836
Enrollment
Unknown
Registered
2025-02-07
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-02-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Duchenne muscular dystrophy

Interventions

Sponsors

West China Second Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
5 Years to 30 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosed with muscular dystrophy through genetic testing and muscle biopsy; (2) No metallic implants in the body, suitable for MRI scanning; (3) No history of organic brain disease; (4) No history of neurological or psychiatric disorders; (5) Understand the potential risks and benefits, agree to participate in the study, comprehend the research procedures, and consent to complete follow-up visits and comply with the study protocol requirements.

Exclusion criteria

Exclusion criteria: (1) Presence of contraindications for MRI scanning; (2) History of taking antipsychotic medications or having taken sedative medications within the past 2 weeks.

Design outcomes

Primary

MeasureTime frame
brain structure;brain function;

Secondary

MeasureTime frame
genomics;

Countries

China

Contacts

Public ContactHuayan Xu

West China Second Hospital, Sichuan University

xuhuayan89@sina.com+86 158 8240 8848

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026