About this trial
Intrauterine devices (IUDs) are highly effective to prevent pregnancy when used for emergency contraception (following unprotected intercourse in the last 3 days), but data are lacking for people who desire an etonogestrel (ENG) contraceptive implant in this situation. This proposal will identify the most effective way to start an implant for emergency contraception using a randomized controlled trial comparing pregnancy risk between those receiving the implant vs. the implant plus oral emergency contraception (EC). Data from this project will inform clinical practice and add another option, the implant, for those desiring a long acting, highly effective contraceptive method when they present for emergency contraception.
Eligibility criteria
Qualifiers
Between 18-35 years old
Unprotected intercourse within 72 hours
Biologically capable of pregnancy (intact uterus without prior sterilization surgery
Fluent in English and/or Spanish
Disqualifiers
Current pregnancy (+urine pregnancy test in clinic)
Breastfeeding
Contraindication to ENG or LNG based on CDC MEC/SPR
Sterilization, hysterectomy, or has an IUD or contraceptive implant in place
Trial design
Treatments tested in this trial
- Etonogestrel implant with Oral Levonorgestrel emergency contraception 1.5mg
- Etonogestrel implant with oral placebo
Treatment groups
Sponsors and collaborators
Lori Gawron
Lead sponsor
University of Utah
Sponsor institution
Planned Parenthood Association of Utah
Collaborator