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 @ 4:19 PM
Ignite Modification Date:
2025-12-24 @ 4:19 PM
NCT ID:
NCT01710566
Eligibility Criteria:
Inclusion Criteria:
* Pregnant women planning vaginal delivery with a trained study provider at a PHC who are eligible to participate in research according to national guidelines and able to provide informed consent.
Exclusion Criteria:
* Women not delivering in study catchment area with a trained study provider will not be eligible to participate in the trial.
* Women with known contraindications to prostaglandins, including misoprostol will also be excluded.
* Women delivering in a facility that currently routinely administers prophylactic oxytocin to women in the third stage labor will also be excluded.
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT01710566
Study Brief:
Protocol Section:
NCT01710566