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Impact of Progestin-only Contraception on Bleeding Patterns in Individuals Initiating GATT

Recruiting
Conditions
Gender
Contraception
Registration Number
NCT06230770
Lead Sponsor
University of California, San Diego
Brief Summary

Gender diverse individuals who use gender-affirming testosterone therapy (GATT) to reduce gender dysphoria may also use progestins for contraception and to manage or suppress uterine bleeding. Research is limited, however, regarding expected bleeding patterns for individuals who choose to initiate GATT concurrently with a progestin. Clinicians who prescribe GATT do not have sufficient data to adequately counsel patients on side effects of concurrent progestin use and therefore extrapolate from studies conducted in cisgender women. This study is a prospective cohort study evaluating bleeding patterns and satisfaction among patients initiating GATT with or without concurrent initiation of a progestin contraceptive. The results from this study will enable clinicians to more accurately counsel patients using GATT on how the use of a progestin might affect their bleeding and whether this differs by progestin method.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
160
Inclusion Criteria
  • English-speaking currently have a uterus and ovaries
  • desire to initiate GATT
  • potential desire to initiate a progestin (within 14 days of GATT initiation)
Exclusion Criteria
  • previous gender-affirming surgery to remove their uterus and/or ovaries

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mean days bleeding or spottingStart of GATT to 30 days

mean number of days of bleeding or spotting during the 30 days after GATT initiation

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of California San Diego

🇺🇸

San Diego, California, United States

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