Clinical trial
Hyperekplexia in Patients With Loss-of-function CTNNB1 Mutation
NCT05168969 is registered in ClinicalTrials.gov with Centre Hospitalier Universitaire de Saint Etienne as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Hyperekplexia in Patients With Loss-of-function CTNNB1 Mutation
- Lead sponsor
- Centre Hospitalier Universitaire de Saint Etienne
- Phase
- Observational
- Overall status
- Completed
- Start date
- July 2, 2022
- Completion date
- December 10, 2022
- Enrollment
- 10 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
ctnnb1 gene mutation, hyperekplexia