RecruitingPhase 2NCT07201402

Long Term Evaluation of Scapular-inserted Contraceptive Implants

Prospective Long-term Study of Etonogestrel Contraceptive Implant Insertion at an Alternative Scapular Site


Sponsor

Yale University

Enrollment

62 participants

Start Date

May 8, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to evaluate long-term outcomes when the etonogestrel contraceptive implant is inserted at an alternative site located over the scapular. The study will evaluate the pharmacokinetics (i.e., drug levels) and side effect profiles of participants who have an etonogestrel contraceptive implant inserted at this alternative scapular site over the course of at least two years.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Scapular-site insertion of etonogestrel contraceptive implant for people with contraception. The study is currently recruiting participants at 2 locations. People eligible for this study include women aged 18 Years to 45 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGScapular-site insertion of etonogestrel contraceptive implant

Participants will undergo insertion of the etonogestrel contraceptive implant subdermally over the inferior edge of their non-dominant scapula


Locations(2)

University of Colorado Anschutz Medical Campus

Aurora, Colorado, United States

Yale University School of Medicine

New Haven, Connecticut, United States

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NCT07201402


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