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Nexplanon Extension Trial Study

Primary Objective

This study is being done to look at the safety, tolerability, and effectiveness of the Nexplanon implant beyond 3 years usage in preventing pregnancy. We are also interested in how extending its usage beyond the current FDA approval of 3 years affects the menstrual cycle and whether complications arise once it is removed.

Study category: Healthy Volunteers

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Description

-11 visits over 27 months -Physical exam, pelvic exam, Pap smear (if needed), STI screening -Blood draws -Daily e-diary completion

Details
Age

18 to 35 years

Eligibility

? Age: 18-35 years ? Sexually Active ? Must have a palpable implant in place (for at least 2 years, no longer than 3 years by the time of enrollment)

Type of Study

Device Feasibility

Compensation

1500

Location

Comprehensive Women's Health Center

Principal Investigator
Rebecca Cohen,  MD

Rebecca Cohen, MD

Resources

Study ID

Protocol Number: 20-2734

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