Clinical Interest of a Genetic Diagnosis in Early Infant Epilepsy, Paraclinical and Therapeutic Management, and Psychological Impact of Families

NCT05455333 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 75

Last updated 2022-08-12

No results posted yet for this study

Summary

To determine the paraclinical and therapeutic interest of genetic diagnosis in early onset epilepsy.

Conditions

  • Early Infant Epilepsy

Interventions

OTHER

Questionnaires

Sends and returns questionnaires to families.

Sponsors & Collaborators

  • University Hospital, Strasbourg, France

    lead OTHER

Eligibility

Max Age
12 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-08-31
Primary Completion
2022-08-31
Completion
2022-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05455333 on ClinicalTrials.gov