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 @ 9:10 PM
Ignite Modification Date:
2025-12-24 @ 9:10 PM
NCT ID:
NCT06680804
Eligibility Criteria:
Inclusion Criteria:
* • Age from 20 to 40 years.
* Time interval more than 1.5 years from previous caesarean section.
* Single viable full-term pregnancy in vertex presentation.
* Reactive cardiotocography (CTG) on admission.
* Spontaneous labor onset.
* Clinically adequate pelvis.
* Single fetus
* Average AFI fetus
Exclusion Criteria:
* • Women with previous upper segment cesarean section or hysterotomy scar.
* Any obstetric complications such as fetal malpresentation, placenta previa, or medical disorders like diabetes mellitus or preeclampsia.
* Presence of any signs and symptoms of scar dehiscence or ruptured uterus, known uterine fibroid or anomaly.
* Suspected fetal macrosomia (weight more than 4 kg).
* Multifetal pregnancy.
* Parturient women who refused the trial of vaginal birth after caesarean section.
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
40 Years
Study:
NCT06680804
Study Brief:
Protocol Section:
NCT06680804