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 @ 2:41 AM
Ignite Modification Date:
2025-12-25 @ 2:41 AM
NCT ID:
NCT02412033
Eligibility Criteria:
Inclusion Criteria:
1. Include those who delivered by CS .
2. Who accept to participate in the study.
3. Desire IUD placement.
4. Negative pregnancy test.
5. No history or current history of pelvic inflammatory disease.
6. No current cervicitis.
7. No contraindication to IUD insertion (less than 4 week post partum,gynecological malignancy,unexplained vaginal bleeding and pregnancy).
Exclusion Criteria:
1. Any contraindication to IUD .
2. Current pregnancy.
3. Uterine anomaly.
4. Undiagnosed abnormal uterine bleeding.
5. Allergy to misoprostol.
6. Patients contraindicated to administration of misoprostol.
7. Women who delivered vaginally.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT02412033
Study Brief:
Protocol Section:
NCT02412033