CrCest Study in Primary Mitochondrial Disease
Enrolling by invitation
Conditions studied: Mitochondrial Diseases
In brief
The purpose of this study is to perform a "muscle phenotyping" magnetic resonance imaging (MRI) assessment in patients receiving clinical care at the Children's Hospital of Philadelphia (CHOP) for mitochondrial disease that is either suspected (based on clinical presentation) or has a definite genetic diagnosis. The MRI assessment quantifies skeletal muscle oxidative phosphorylation (OXPHOS) capacity. Investigators hope that this study will contribute to our current knowledge of mitochondrial diseases and this study will help create a new diagnostic tool for use in both clinical care and in clinical trials.
Key facts
- Study ID
- NCT04734626
- Run by
- Children's Hospital of Philadelphia
- People needed
- 230
- Starts
- 2021-05-25
- Expected to finish
- 2028-12-31
- Last updated by the study team
- 2026-01-14
Who can join
Age: 7 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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