CompletedNCT05615571
Testing of NBIA Genes: Analysis of Genetic Heterogeneity and Validation of Mitochondrial Markers for Assessing Causality of Sequence Variants.
Studying Neurodegeneration with brain iron accumulation
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospital, Bordeaux
- Principal Investigator
- Patricia FERGELOT MAURINUniversity Hospital, Bordeaux
- Intervention
- Establishment of mitochondrial markers(genetic)
- Enrollment
- 70 enrolled
- Eligibility
- All sexes
- Timeline
- 2018 – 2020
Study locations (1)
- Centre Hospitalier Universitaire de Bordeaux, Talence, France
Collaborators
Institut National de la Santé Et de la Recherche Médicale, France
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT05615571 on ClinicalTrials.gov