Want to participate in a research study on a nonhormonal birth control method?

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 wcfpr@jhmi.edu.

PI: Anne E. Burke, MD, MPH
Study number: IRB00128521