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 @ 7:40 PM
Ignite Modification Date:
2025-12-24 @ 7:40 PM
NCT ID:
NCT01990703
Eligibility Criteria:
Inclusion Criteria:
* Healthy, 18-40 year old pregnant women
* Intend to breastfeed
* Desire the LNG IUD as their method of contraception
* Agree to be randomized to early versus standard postpartum insertion
* Have delivered a healthy term infant (37 weeks gestation)
* Willing to complete all study related procedures, visits and questionnaires
Exclusion Criteria:
* Chorioamnionitis
* Obstetric complications including transfusion
* Severe pregnancy induced hypertension
* Prolonged hospitalization
* Coagulopathy
* Liver disease
* Undiagnosed genital bleeding, or other relative contraindication to LNG IUD insertion (known or suspected pregnancy, uterine cavity abnormality, known, suspected, or history of breast cancer, or hypersensitivity to any of the components in the LNG IUD).
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
40 Years
Study:
NCT01990703
Study Brief:
Protocol Section:
NCT01990703