This study will evaluate the contraceptive efficacy, safety, and tolerability of a copper intrauterine device.
- Participation requires multiple, frequent study visits over a 38-month period.
- Visits will occur at Johns Hopkins Bayview Medical Center.
- Volunteers will be compensated for participation and travel.
- Women must be healthy, age 18 or older, and have regular menstrual cycles.
If you are interested in participating, call 410-550-8506 or email email@example.com.
PI: Anne E. Burke, MD, MPH
Study number: IRB00128521