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:
2025-12-26 @ 1:18 PM
Ignite Modification Date:
2025-12-26 @ 1:18 PM
NCT ID:
NCT03544606
Eligibility Criteria:
Inclusion Criteria:
* Singleton pregnancy.
* Cephalic presentation.
* Bishop score \< 6.
* Average size of the fetus.
* Adequate pelvic dimensions.
* Term or post-term pregnancies with an indication for labor induction either maternal or fetal.
Exclusion Criteria:
* • Previous uterine scar.
* Patients with regular uterine contractions.
* Malpresentation.
* Multifetal gestation.
* Prelabour rupture of membranes.
* Established fetal distress.
* Indication for CS, e.g. Major degree of cephalopelvic disproportion and fetal macrosomia.
* Antepartum hemorrhage.
* Active genital herpes infection.
* Severe maternal illness (e.g. severe preeclampsia).
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
35 Years
Study:
NCT03544606
Study Brief:
Protocol Section:
NCT03544606