Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:34 AM
Ignite Modification Date:
2025-12-25 @ 2:34 AM
NCT ID:
NCT05317234
Eligibility Criteria:
Inclusion Criteria:
* Child between 2 and 15 years old with a clinical diagnostic of cerebral paralysis with unilateral or bilateral somatic involvement
* Child born from 34 SA
* Agreement of the legal representatives for the genetic study
* Both parents available for a parental genetic study (if detection of class 3 variant)
* Affiliation to the social security system
Exclusion Criteria:
* Genetic syndrome identified or malformative or infectious etiologies identified
* Neonatal encephalopathy criteria in a clear obstetrical etiological context responsible for major perinatal anoxia with Sarnat 2 or 3
* Unilateral motor disorders in perinatal stroke of identified etiology (coagulation anomaly)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
2 Years
Maximum Age:
15 Years
Study:
NCT05317234
Study Brief:
Protocol Section:
NCT05317234