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 @ 12:41 PM
Ignite Modification Date:
2025-12-24 @ 12:41 PM
NCT ID:
NCT00670761
Eligibility Criteria:
Inclusion Criteria:
* If no ultrasound used:
1. Past or present history of vaginal bleeding during pregnancy; and
2. Open cervical os.
* If ultrasound used:
1. Past or present history of vaginal bleeding during pregnancy; and
2. Evidence of incomplete abortion with substantial debris in the uterus.
All women would have been advised to have surgical evacuation of the uterus if misoprostol was not available.
* Willing to provide contact information for purposes of follow-up.
* In Tanzania: 18 years of age or over or parental permission
* In Mozambique: 21 years of age or over or parental permission
* In Moldova: 18 years of age or over
* In Madagascar: 18 years of age or parental permission
* In Vietnam: reproductive age
Exclusion Criteria:
* Contraindications to the study drug;
* Uterine size larger than 12 weeks L.M.P. at time of presentation for care.
* Signs of severe infection, defined as at least one of the following of:
1. foul smelling discharge,
2. fever \> 39 degrees C ,
3. pulse \>110/min;
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT00670761
Study Brief:
Protocol Section:
NCT00670761