Etonogestrel Implant as Emergency Contraception

Official title

Etonogestrel Implant as Emergency Contraception: A Pilot Pharmacodynamic Study

Overview

The investigators propose a single site, single arm, open label mechanism of action pharmacodynamic pilot study of etonogestrel implant insertion prior to an luteinizing hormone (LH) surge. The investigators will evaluate ovulation rates via serum levels of reproductive hormones and transvaginal ultrasound findings following placement of an etonogestrel implant once the dominant follicle reaches a size of 15mm or greater, but prior to an LH surge, in persons with prior documented regular cycles and confirmed ovulation. The researchers' hypothesis is that ovulation will be inhibited if the etonogestrel implant is placed prior to an LH surge. Based on data from the Food and Drug Administration label for Nexplanon, etonogestrel rises to levels associated with ovulation suppression within 8 hours of placement. Given this rapid increase, it is therefore plausible to assume that ovulation can be inhibited by the implant if placed prior to an LH surge. This study is novel as there have been no published studies evaluating an etonogestrel implant for this indication. The contribution of this proposed research to the literature is significant because current recommendations from the Center for Disease Control (CDC) regarding timing of etonogestrel implant placement are stringent and not patient-centered. Any day insertion of the etonogestrel implant is supported by retrospective data and this pharmacodynamic data would further support the literature for any day insertion without the need for additional emergency contraception. If results support the investigators' hypothesis, it could increase access to contraception and decrease duplicative therapy.

Interventions

• Drug Etonogestrel implant
  Implant insertion in second menstrual cycle prior to ovulation

Primary outcome measures

• Serum progesterone [Time frame: 7 days]
• Ovarian follicle size [Time frame: 7 days]

Secondary outcome measures (1)

• Luteinizing hormone [Time frame: 7 days]

Eligibility criteria

Inclusion criteria

• BMI less than or equal to 28kg/m2
• Intact uterus with at least one ovary
• Regular menstrual cycles that occur every 21-35 days
• If patient is postpartum or post-second trimester abortion, 3 menses (2 cycles) must have occurred prior to enrollment
• If patient had a first trimester abortion or pregnancy loss, she must have one spontaneous menses prior to enrollment
• Desires insertion of an etonogestrel contraceptive implant for contraception
• Not currently pregnant or trying to become pregnant
• Willing to abstain from medications and supplements known to induce/inhibit CYP3A4 during the study

Exclusion criteria

• Have a known hypersensitivity or contraindications to etonogestrel.
• Medical conditions that affect liver function (e.g., hepatitis, cirrhosis; assessed via participant self-report)
• Known or suspected current alcohol dependence syndrome or any illicit drug use that may affect the metabolism of the etonogestrel.
• Uncontrolled thyroid disorder.
• Use of long-acting injectable hormonal contraceptive within the past 9 months
• Current use of hormonal oral, patch, intravaginal, or intrauterine contraception

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation

N/A

Model

Single group

Masking

Open label

Primary purpose

Basic science

Study locations

United States · 1 center

• University of Colorado Denver — Aurora

Identifiers

NCT: NCT05237141 · 21-5026

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗