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 @ 2:14 AM
Ignite Modification Date:
2025-12-25 @ 2:14 AM
NCT ID:
NCT01272960
Eligibility Criteria:
Inclusion Criteria:
* 14-45 years
* Vaginal Delivery at Barnes-Jewish Hospital
* Sexually active with male partner
* No tubal ligation/hysterectomy
* Not currently using contraception
* Desire reversible contraception
* Reside in St. Louis City/County
* Requests Mirena(R) intrauterine device for contraception
Exclusion Criteria:
* Allergy to Mirena(R) system
* Cesarean delivery
* Cervical cancer, breast cancer
* Active liver disease
* Untreated cervicitis
* Uterine anomaly/fibroids preventing Mirena(R) placement
* Delivery \<36 weeks
* Chorioamnionitis
* Prolonged rupture of membranes (\>18 hours)
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
14 Years
Maximum Age:
45 Years
Study:
NCT01272960
Study Brief:
Protocol Section:
NCT01272960