NCT05168969View on ClinicalTrials.gov

Hyperekplexia in Patients With CTNNB1 Mutation

CompletedOBSERVATIONAL
Enrollment

10

Participants

Timeline

Start Date

July 2, 2022

Primary Completion Date

December 10, 2022

Study Completion Date

December 10, 2022

Conditions
HyperekplexiaCTNNB1 Gene Mutation
Interventions
OTHER

Questionnaire

The families and health care providers will be invited to fill in a questionnaire related to hyperekplexia (clinical, pharmacological, and genetic data).

Trial Locations (1)

42055

Chu Saint-Etienne, Saint-Etienne

All Listed Sponsors
lead

Centre Hospitalier Universitaire de Saint Etienne

OTHER