CClinicalTrials.gg
RecruitingNCT06162611Updated Jun 2, 2026

Etonogestrel (ENG) Implant Insertion for Emergency Contraception With Oral Levonorgestrel (LNG) vs Placebo

A Phase 4 interventional study of Etonogestrel implant with Oral Levonorgestrel emergency contraception 1.5mg and Etonogestrel implant with oral placebo in Emergency Contraception, sponsored by Lori Gawron. Recruiting at 1 site in United States. Open to female participants aged 18 Years to 35 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-06-02.

Sponsored by Lori Gawron · Phase 4, Interventional, and Prevention

From the registry’s dates

  • Started Nov 2023; still recruiting 2 years 11 months later.
Phase
Phase 4
Study type
Interventional
Enrollment
790
Allocation
Randomized
Ages
18 Years to 35 Years
Sex
Female
01

Study summary

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.

Read the detailed description

Oral emergency contraception (EC), is commonly used after recent unprotected intercourse to avoid undesired pregnancy, but does not provide ongoing contraception. Rigorous data allow for use of intrauterine devices (IUDs) as both EC and ongoing contraception, but EC efficacy data on use of the etonogestrel (ENG) implant, is lacking. The CDC Selected Practice Recommendations for Contraceptive Use support initiation of the ENG implant if oral levonorgestrel (LNG) is given concomitantly for EC. This recommendation lacks supporting evidence and serves as a barrier to method initiation, as oral LNG is not typically available in clinics when clients desire an implant. Additionally, oral LNG efficacy decreases in higher body mass index (BMI) users and the role of BMI on efficacy with co-administered oral LNG and the ENG implant is unknown. As the ENG implant is also a synthetic progestogen with a rapid rise and consistent systemic levels, it could plausibly serve as stand-alone EC or increase the efficacy of oral LNG with co-administration. Moreover, the EC mechanism of action, which is related to ovulatory suppression with oral EC, may differ if the implant is initiated with or without oral LNG, impacting efficacy in mid cycle users. This study addresses the following research gaps around use of the ENG implant for EC that serve as barriers to provider comfort with these options: efficacy with and without oral LNG, efficacy differences by BMI, and ovulation frequency with and without oral LNG. The investigators propose a randomized, placebo-controlled, non-inferiority study to determine if the ENG implant alone is no worse than the ENG implant + oral LNG for EC, using a 3.5% non-inferiority margin. The investigators will include clients who present to Planned Parenthood Association of Utah clinics with report of unprotected intercourse within 72 hours who desire EC. Eligible EC clients interested in an implant with a negative pregnancy test will be allocated 1:1 to a study group: (1) ENG implant + oral LNG or (2) ENG implant + placebo. Our experienced research staff will follow up with participants for 4-week efficacy data as primary outcome. Our aims include: (1) To compare the efficacy of the ENG Implant + oral LNG to the ENG Implant + placebo for EC in 790 participants assessed by pregnancy status four weeks after implant placement, (2) To compare pregnancy risk by BMI category (the investigators anticipate half of the 790 participants will have a BMI ≥25) between and within the ENG Implant + oral LNG and the ENG Implant + placebo groups, and (3) To evaluate ovulation frequency within 5 days of insertion of ENG Implant + oral LNG or ENG implant + placebo in 202 participants who are mid cycle (day 7-14 post menses) at time of enrollment assessed by serum progesterone levels and urine fertility monitor results. Our short-term goal is to expand evidence on the efficacy of implant initiation with or without oral LNG to meet the needs of EC clients. Our long-term goals are to develop evidence-based clinical guidelines to inform global contraceptive practices, allow for equity in long acting reversible contraception counseling at the time of EC, and support reproductive autonomy for people to achieve to their life goals.

02

Conditions studied

  • Emergency Contraception

Keywords

  • contraception
  • etonogestrel implant
  • oral levonorgestrel
03

In context

Lead sponsor

This is the only study on the registry with Lori Gawron as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 35 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • 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
  • Have a regular menstrual cycle (21-35 days)
  • Known last menstrual period (+/- 3 days)
  • Working (cell) phone number
  • Willing to comply with the study requirements
  • Willing to abstain from any CYP3A4 inducer for 5 days

Exclusion criteria

Exclusion Criteria:

  • 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
  • Vaginal bleeding of unknown etiology
  • Previous use of EC in same cycle
  • Allergy to LNG or ENG
  • History of intolerance/ side effects with ENG Implant
  • Current (past 7 days) use of any CYP3A4 inducer
  • Plan to use any other steroid hormone in the next 4 weeks (testosterone, estrogen, progesterone)
  • Ended a pregnancy at or under 20 weeks gestational age within last 2 weeks
  • Ended a pregnancy over 20 weeks gestational age in last 6 weeks
  • Use of any injectable hormonal contraceptive (Depo-Provera) in the last 15 weeks
  • Use of any oral EC, contraceptive pills, patches, vaginal rings, or an IUD or Implant in the last 2 weeks
05

Study design

Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
790 participants (estimated)

Study arms

  • Active comparator
    Etonogestrel contraceptive implant with oral levonorgestrel

    Patients will be randomized 1:1 to each arm and will receive the contraceptive implant with a same-day encapsulated pill with either oral levonorgestrel 1.5mg

    Drug: Etonogestrel implant with Oral Levonorgestrel emergency contraception 1.5mg

  • Placebo comparator
    Etonogestrel contraceptive implant with placebo

    Patients will be randomized 1:1 to each arm and will receive the contraceptive implant with a same-day encapsulated pill with placebo X 1 dose

    Device: Etonogestrel implant with oral placebo

Interventions

  • DrugEtonogestrel implant with Oral Levonorgestrel emergency contraception 1.5mg

    Single pill of oral levonorgestrel 1.5mg X 1 dose (e.g. Plan B) same day as contraceptive implant insertion

  • DeviceEtonogestrel implant with oral placebo

    Single pill of placebo same day as contraceptive implant insertion

06

What researchers measure

Primary outcomes

  1. Efficacy of the etonogestrel contraceptive implant with placebo for emergency contraception

    Pregnancy rate = number of pregnancies / participants in the placebo arm

    Time frame: 1 month after enrollment

  2. Efficacy of the etonogestrel contraceptive implant with placebo for emergency contraception by BMI category

    Pregnancy rate = # of pregnancies / participants in the placebo arm stratified by BMI category

    Time frame: 1 month after enrollment

  3. Efficacy of the etonogestrel contraceptive implant with oral levonorgestrel for emergency contraception

    Pregnancy rate = # of pregnancies / participants in the oral levonorgestrel arm

    Time frame: 1 month after enrollment

  4. Efficacy of the etonogestrel contraceptive implant with oral levonorgestrel for emergency contraception by BMI category

    Pregnancy rate = # of pregnancies / participants in the oral levonorgestrel arm stratified by BMI category

    Time frame: 1 month after enrollment

  5. Ovulation frequency within 5 days of implant insertion in the oral levonorgestrel arm

    Incidence of ovulation within 5 days after implant insertion measured by urine fertility monitor results and serum progesterone

    Time frame: 5 days after implant insertion

  6. Ovulation frequency within 5 days of implant insertion in the placebo arm

    Incidence of ovulation within 5 days after implant insertion measured by urine fertility monitor results and serum progesterone

    Time frame: 5 days after implant insertion

Secondary outcomes

  1. Implant continuation

    Participants continuing implant use at one month as a proportion of all participants having successful placement of implant at study entry. Measured by probabilities estimated using Kaplan-Meier approach.

    Time frame: 4 weeks after insertion

  2. Implant satisfaction

    Likelihood of satisfaction by study group using ordinal regression. Measured by 5-point ordinal scale (5-point ordinal scale: (1) very unsatisfied, (2) unsatisfied, (3) neutral, (4) satisfied, (5) very satisfied). Measured by

    Time frame: 4 weeks after insertion

07

Study locations

1 of 1 sites recruiting
  • Planned Parenthood Association of Utah
    Salt Lake City, Utah 84102, United States
    • Corinne Sexsmith · Contact
    • David Turok, MD, MPH · Sub investigator
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06162611
Lead sponsor
Lori Gawron
Collaborators
Planned Parenthood Association of Utah
Responsible party
Lori Gawron (Associate Professor OBGYN, University of Utah) — Sponsor-investigator
First posted
Dec 8, 2023
Start date
Nov 6, 2023
Primary completion
Apr 30, 2028 (estimated)
Completion
May 31, 2028 (estimated)
Last update
Jun 2, 2026

Study contacts

Corinne Sexsmith, MPH
Contact
corinne.sexsmith@hsc.utah.edu
801-213-2419
Sarah Elliott, MPH
Contact
sarah.elliott@hsc.utah.edu
801-646-7066
Lori Gawron, MD, MPH
principal investigator · University of Utah

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
Yes
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion