Natural History in Primary Mitochondrial Myopathies
NCT05653544 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 150
Last updated 2025-09-16
Summary
This is a longitudinal study in a cohort of patients with a genetic diagnosis of Primary Mitochondrial Myopathy to describe the natural history of the disease and identify clinical, biochemical, molecular, and radiological variables that allow evaluation of the severity and progression of the disease and may be useful in future clinical trials.
Conditions
- Primary Mitochondrial Myopathies
Sponsors & Collaborators
-
Cristina Domínguez González
lead OTHER
Eligibility
- Min Age
- 16 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-01-01
- Primary Completion
- 2026-06-01
- Completion
- 2026-12-31
Countries
- Spain
Study Locations
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