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 @ 4:46 PM
Ignite Modification Date:
2025-12-24 @ 4:46 PM
NCT ID:
NCT00116350
Eligibility Criteria:
Inclusion Criteria:
* Vaginal delivery
* Postpartum hemorrhage due to suspected uterine atony
* Depending on study group: administration of prophylactic uterotonics in third stage of labor
Exclusion Criteria:
* Known allergy to misoprostol or other prostaglandin
* C-section for current delivery
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00116350
Study Brief:
Protocol Section:
NCT00116350