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Nexplanon Use in Women Primarily Choosing a Combined Oral Contraceptive: a Multicenter Trial

Study category: Women's Health

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Description

1. Women who desire a COC for contraception will be willing to initiate and continue an ENG implant as a continuous back-up method. 2. Women using a COC concomitantly with ENG implant will have low rates (<5%) of ENG discontinuation for bleeding complaints. 3. A high percentage of women in the study will still be using the ENG implant after 52 weeks (1 year).

Details
Age

Adult

Eligibility

Women 18 years and older currently using COCs or who have a COC prescription and are intending to initiate COCs for contraception Exclusion Criteria. Women who have contraindications to using a COC or a contraceptive implant (Category 3 or 4 in the CDC Medical Eligibility Criteria [MEC]) o Because the CDC MEC are continuously revised, we will refer to the most updated criteria at http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5904a3.htm Women who are currently participating in a clinical trial or have participated within the past 30 days. Less than 2 weeks from the end of a pregnancy.

Women 18 years and older currently using COCs or who have a COC prescription and are intending to initiate COCs for contraception Exclusion Criteria. Women who have contraindications to using a COC or a contraceptive implant (Category 3 or 4 in the CDC Medical Eligibility Criteria [MEC]) o Because the CDC MEC are continuously revised, we will refer to the most updated criteria at http://www.cdc.gov/mmwr/preview/mmwrhtml/rr5904a3.htm Women who are currently participating in a clinical trial or have participated within the past 30 days. Less than 2 weeks from the end of a pregnancy.

Type of Study

Device Feasibility

Location

Comprehensive Women's Health Center

Principal Investigator
Rebecca Cohen,  MD, MPH

Rebecca Cohen, MD, MPH

Study ID

Protocol Number: 20-1945

More information available at ClinicalTrials.gov: NCT04423055

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