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Clinical Trial Summary

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).


Clinical Trial Description

Objective: 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). Secondary Objectives: To determine if participants initiating the contraceptive implant who are also provided COCR are more likely than participants receiving standard counseling to: 1. report higher levels of satisfaction with their contraceptive implant at one year following initiation 2. require less clinical follow-up and clinical resources in the year following initiation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04828824
Study type Interventional
Source University of Colorado, Denver
Contact Jeanelle Sheeder, PhD
Phone (303) 724-2272
Email jeanelle.sheeder@cuanschutz.edu
Status Recruiting
Phase Phase 4
Start date June 18, 2021
Completion date December 31, 2025

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