Premature Discontinuation of Contraceptive Implants

Description

To compare rates of etonogestrel implant discontinuation in implant initiators who are given advance provision of combined oral contraceptive pills (COCs) and a bleeding rescue regimen (COCR intervention) to participants given standard counseling (comparator).

Conditions

Contraception Behavior

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Study Overview

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Study Details

Study overview

To compare rates of etonogestrel implant discontinuation in implant initiators who are given advance provision of combined oral contraceptive pills (COCs) and a bleeding rescue regimen (COCR intervention) to participants given standard counseling (comparator).

Reduction of Premature Discontinuation of Contraceptive Implants by Advance Provision of an OCP-based Participant Intervention: Randomized Clinical Trial

Premature Discontinuation of Contraceptive Implants

Condition
Contraception Behavior
Intervention / Treatment

-

Contacts and Locations

Aurora

Children's Hospital Colorado, Aurora, Colorado, United States, 80045

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. You are between ages of 14 to 22.9 years.
  • 2. Started etonogestrel implant for the first time and have never used the implant before.
  • 1. There is any contraindication to estrogen containing birth control.
  • 2. Desire of pregnancy in next 12 months.
  • 3. Plans to move from the area in next 12 months and is not able to come to the clinic.

Ages Eligible for Study

14 Years to 23 Years

Sexes Eligible for Study

FEMALE

Accepts Healthy Volunteers

Yes

Collaborators and Investigators

University of Colorado, Denver,

Study Record Dates

2025-12-31