FindTrial
Sign In

Mitochondrial myopathy caused by TOP3A gene mutation characterized by dilated cardiomyopathy (DCM)

Mitochondrial myopathy caused by TOP3A gene mutation characterized by dilated cardiomyopathy (DCM)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117173
Enrollment
Unknown
Registered
2026-01-20
Start date
2023-05-30
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

Dilated Cardiomyopathy

Interventions

Observation group:Uninvolved

Sponsors

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
9 Years to 11 Years

Inclusion criteria

Inclusion criteria: None

Exclusion criteria

Exclusion criteria: 1.TOP3a gene mutation is not the causative gene; 2.without mitochondrial myopathy;

Design outcomes

Primary

MeasureTime frame
state of existence;Peripheral blood mitochondrial DNA qPCR;—

Countries

China

Contacts

Public ContactYipu Zhang

Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine

zhangyipu920@163.com+86 21 3862 6161

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026