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 @ 9:49 PM
Ignite Modification Date:
2025-12-24 @ 9:49 PM
NCT ID:
NCT01816932
Eligibility Criteria:
Inclusion criteria
* Women aged 18 and over
* Was pregnant within the last 10 weeks
* Interested in using the etonogestrel implant for contraception
* Willing to have investigators come to the home for an insertion visit
* Presenting to University Hospitals for delivery or contraception.
* Has running water and a working bathroom in the home
* Has a safe and private location in the home for the implant to be inserted
Exclusion criteria
* Current or history of thrombosis or thromboembolic disorders
* Liver tumors or active liver disease
* Undiagnosed abnormal genital bleeding
* Known or suspected breast cancer or history of breast cancer
* Allergic reaction to components (ethylene vinylacetate, etonogestrel, barium sulfate) of etonogestrel implant or local anesthetics
* Women currently taking hepatic enzyme inducers including but not exclusive to barbiturates, bosentan, carbamazepine, felbamate, griseofulvin, oxcarbazepine, phenylbutazone, phenytoin, rifampin, topiramate, protease inhibitors, and St. John's wort
* Uncontrolled hypertension
* Housing located greater than 10 miles from University Hospitals Center for Women's Health
* The location of the home is in a place that would not be safe for investigators
* Participant is homeless
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT01816932
Study Brief:
Protocol Section:
NCT01816932