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 @ 12:12 PM
Ignite Modification Date:
2025-12-24 @ 12:12 PM
NCT ID:
NCT04676061
Eligibility Criteria:
Inclusion Criteria:
* Between the ages of 18-48
* Between ages of 14-17 with parental/guardian permission
* Women desiring placement of Nexplanon™
* Willing to keep a daily symptom calendar
* Keep appointments
* Women not desiring to become pregnant in the next 2 years
Exclusion Criteria:
* Known or suspected Pregnancy
* Less than 8weeks postpartum
* Menarche less than two years ago
* Current or past history of thrombosis or thromboembolic disorders
* Hepatic tumors (benign or malignant)
* Active liver disease
* Undiagnosed abnormal genital bleeding
* Undiagnosed headaches
* Known or suspected carcinoma of the breast or personal history of breast cancer
* Hypersensitivity to any of the components in Nexplanon™
* BMI greater than 40
* Depomedroxyprogesterone acetate injection in the previous 12 weeks
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
14 Years
Maximum Age:
48 Years
Study:
NCT04676061
Study Brief:
Protocol Section:
NCT04676061