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 @ 2:03 AM
Ignite Modification Date:
2025-12-25 @ 2:03 AM
NCT ID:
NCT00951860
Eligibility Criteria:
Inclusion Criteria:
* Every child born in the CHU of Saint-Étienne (inborn), any term of its birth, in the hospital neonatal unit at the time of registration (after 37 weeks corrected for prematurity) or in the maternity
* Written consent signed by parents
* Parents affiliated in a Social Security regimen
Exclusion Criteria:
* History of intrafamilial dysautonomia
* Heart malformation, congenital abnormality of the brainstem
* Permanent troubles of heart rate
* Any therapy at the time of the study or made in the weeks preceding the study, referred to cardiac or respiratory or known to alter the activity of the ANS
* General anesthesia within 2 weeks prior to registration
Healthy Volunteers:
True
Sex:
ALL
Maximum Age:
1 Week
Study:
NCT00951860
Study Brief:
Protocol Section:
NCT00951860