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:
2025-12-24 @ 6:28 PM
Ignite Modification Date:
2025-12-24 @ 6:28 PM
NCT ID:
NCT03572868
Eligibility Criteria:
Inclusion Criteria:
* 2nd or the 3rd trimester ultrasound examination realized at the hospital "Femme Mère Enfant" in Lyon between 2008 and 2015
* Isolated Transverse cerebellar diameter \<5th centile
* Parents who received the information and did not object to participate to the study
Exclusion Criteria:
* Decreased Transverse cerebellar diameter with associated malformations diagnosed during prenatal period
* Family history of neurodevelopmental delay or cognitive impairment
* Preterm delivery (\< 28 WG)
* Severe restriction in growth at birth (\<3e centile)
* Neonatal asphyxia (pH blood cord \< 7)
* Apgar score \< 7 at 5 min of live with transfer to the neonatal intensive care unit
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03572868
Study Brief:
Protocol Section:
NCT03572868