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 @ 2:02 AM
Ignite Modification Date:
2025-12-25 @ 2:02 AM
NCT ID:
NCT04070560
Eligibility Criteria:
Inclusion Criteria:
* Pregnancy week ≥35 + 0
* Singletons
* Expected vaginal delivery
* The woman / couple can adequately assimilate information about the study
* Signed informed consent of both prospective parents
Exclusion Criteria:
* Congenital malformation that complicates resuscitation (such as severe malformation of mouth, pharynx, respiratory system) or which causes the child not to be resuscitated due to internal structural malformations (such as more severe heart failure, diaphragm fractures, etc.)
* The child is born via acute caesarean section after inclusion and opening of study envelope
* placenta abruption / or damage to umbilical cord during childbirth (when circulation through an intact umbilical cord cannot be achieved after birth)
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
35 Weeks
Maximum Age:
42 Weeks
Study:
NCT04070560
Study Brief:
Protocol Section:
NCT04070560