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 @ 4:37 PM
Ignite Modification Date:
2025-12-24 @ 4:37 PM
NCT ID:
NCT03098966
Eligibility Criteria:
Inclusion Criteria:
* Women admitted in labour
* One prior caesarean section
* Singleton pregnancy
* Vertex-presenting fetus
Exclusion Criteria:
* Prior high-risk uterine scar; uterine rupture, classical CS, hysterotomy or myomectomy
* Short inter-delivery interval (\<12 months)
* Complications in the previous CS (e.g. puerperal sepsis)
* Obstetric indication for CS (either elective or emergency):
* Placenta praevia
* Placental abruption
* Documented evidence of cephalopelvic disproportion
* Fetal macrosomia (estimated fetal weight \>4 kg)
* Fetal anomalies interfering with vaginal delivery e.g. hydrocephalus
* Fetal distress or non-reassuring Cardiotocography pattern
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
35 Years
Study:
NCT03098966
Study Brief:
Protocol Section:
NCT03098966