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 @ 3:55 PM
Ignite Modification Date:
2025-12-24 @ 3:55 PM
NCT ID:
NCT03863392
Eligibility Criteria:
Inclusion Criteria:
* Primigravida or Primipara
* Pregnancy between 36 and 42 weeks of gestation.
* A live singleton fetus in cephalic presentation.
* No history of uterine surgery.
* Clinically adequate pelvis.
* Modified Bishop's score \<5.
* Reactive Non stress test (NST) .
Exclusion Criteria:
* •Known hypersensitivity or contraindications to oral misoprostol (uterine surgery).
* Any antenatal medical complications.
* A situation requiring LSCS (Maternal or Fetal) e.g:fetal distress
* Non-reactive NST.
* Patient's refusal to give consent
Healthy Volunteers:
True
Sex:
FEMALE
Study:
NCT03863392
Study Brief:
Protocol Section:
NCT03863392