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 @ 2:08 AM
Ignite Modification Date:
2025-12-25 @ 2:08 AM
NCT ID:
NCT00671060
Eligibility Criteria:
Inclusion Criteria:
* Women presents with spontaneous fetal death
* Gestational age of fetus between 14-28 weeks
Exclusion Criteria:
* Transmural uterine scar;
* Allergies or other contraindications to use of misoprostol;
* Placental abruption with active hemorrhage;
* Complete placenta previa;
* Extreme uterine structural anomalies;
* Or other contraindications to vaginal delivery of the fetus;
* Presentation in active labor (moderate to severe contractions every 10 minutes); or
* Four or more previous deliveries
Healthy Volunteers:
False
Sex:
FEMALE
Study:
NCT00671060
Study Brief:
Protocol Section:
NCT00671060