Actively Recruiting
Mitochondrial Disease-associated ImmunoDeficiencies
Led by University Hospital, Bordeaux · Updated on 2026-02-03
60
Participants Needed
2
Research Sites
204 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study aims at characterizing the immune dysfunctions in patients with mitochondrial diseases. This has prognostic and diagnostic interest as well as potential for the discovery of new therapeutic strategies to alleviate disease burden.
CONDITIONS
Official Title
Mitochondrial Disease-associated ImmunoDeficiencies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participant must weigh more than 30 kilograms
- Participant must be affiliated with or receiving a social security plan
- Participant must have a molecularly confirmed primary mitochondrial disease
- Signed informed consent must be provided by the participant or their legal guardian as appropriate
- Control participants must be matched by age (±5 years) and sex to a mitochondrial disease patient
- Control participants must have no known mitochondrial disease
- Control participants must provide informed and signed consent
You will not qualify if you...
- Pregnant or breastfeeding women
- Refusal to consent to participate in the research
- Patients without a formally identified molecular cause (no genetic analysis performed, or no variant or variant of unknown significance found)
AI-Screening
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Trial Site Locations
Total: 2 locations
1
Chu Bordeaux
Bordeaux, France
Actively Recruiting
2
Hopital Toulouse
Toulouse, France, 31059
Not Yet Recruiting
Research Team
A
Aurélien TRIMOUILLE, MD
CONTACT
J
Johan Garaude, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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