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 @ 12:04 AM
Ignite Modification Date:
2025-12-25 @ 12:04 AM
NCT ID:
NCT01107158
Eligibility Criteria:
Inclusion Criteria:
* Patients undergoing C-section for a dystocia: 2 to 3 hours of stagnation in labor progress are observed (ie no increasing dilation, and uterine contractions less that 3-5 per 10 minutes) in spite of measures taken to overcome dystocia (oxytocin injection and artificial breaking of waters)
* the child is alive
* the child does not have apriori known malformations that could interfere with a vaginal birth
* foetus in cephalic position
* full term pregnancy (\>= 37 weeks of amenorrhea)
* single birth
* patient has signed consent
* patient is affiliated with a social security system
Exclusion Criteria:
* vaginal birth
* programmed C-section
* C-section is chosen because the fetus has a cardia rhythm problem, and there is no stagnation in the labor process
* multiple pregnancy
* the child is in a breech position
* premature birth (\<37 weeks amenorrhea)
* in utero fetal death
* fetal malformation known before birth that could interfere with a vaginal birth
* non french-speaking patient (impossible to correctly inform the patient)
* patient under guardianship
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT01107158
Study Brief:
Protocol Section:
NCT01107158