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 @ 3:29 AM
Ignite Modification Date:
2025-12-25 @ 3:29 AM
NCT ID:
NCT02676505
Eligibility Criteria:
Inclusion Criteria:
All patients admitted in the first stage of labor with cervical dilatation of 4 cm at least:
1. Women age 18-35 years.
2. 37-41 weeks gestation pregnancy.
3. Singleton pregnancy and vertex presentation.
4. Women have no chronic or pregnancy-induced illnesses.
5. Women are in established, spontaneous labor.
Exclusion Criteria:
1. Malpresentation.
2. Women with previous uterine scar.
3. Multiple pregnancy
4. Ante partum hemorrhage.
5. Cephalopelvic disproportion.
6. Women have chronic illnesses.
7. Women with abnormal antenatal period.
8. Patients with foetal distress
9. Premature rupture of membrane
10. Woman having any contraindication to vaginal delivery.
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
35 Years
Study:
NCT02676505
Study Brief:
Protocol Section:
NCT02676505