Feminizing Hormone Therapy and the Rectal Mucosa Immune Environment in Transgender Women
Completed
Conditions studied: HIV Prevention
In brief
The overarching goal of this research study is to achieve a better understanding of the rectal mucosal effects of feminizing hormones in people assigned male sex at birth and currently taking feminizing hormones who have sex with men. Better understanding the rectal mucosa in this population will allow for the optimization of current biomedical HIV prevention interventions and enhance design of future interventions, including an effective HIV vaccine. This study will recruit approximately 520 transgender women who have receptive anal intercourse with men (TGWSM) and cis-gender men into one of two cohorts. Cohort 1 is a cross-sectional study and Cohort 2 is a longitudinal study; enrollment into each cohort is based on participant characteristics.
Key facts
- Study ID
- NCT04531943
- Run by
- Emory University
- People needed
- 285
- Starts
- 2020-10-01
- Expected to finish
- 2024-04-04
- Last updated by the study team
- 2025-06-17
Who can join
Age: 18 and older, up to 59. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Cohort 1, TGWSM using feminizing hormone therapy
- Assigned male sex at birth and currently using feminizing hormone therapy
- Aged 18-59 years
- Able to provide informed consent in the official language of the study site's country
- HIV negative
- Taking feminizing hormone therapy for at least the last 6 months with no change in dose for the last 3 months (i.e. no increase or decrease)
- Feminizing hormone therapy is defined as use of oral, patch, topical, or injection estrogen therapy with or without progesterone therapy in people who were assigned male sex at birth but take feminizing hormones to affirm their current gender identity
- Approximately half of the cohort to be using estrogen therapy alone and half using estrogen+progesterone
- Anti-androgen therapy is permissive, but dose must also be stable for the last 3 months at the time of enrollment
- Willing to undergo peripheral blood and rectal biopsy sampling
- Willing to abstain from receptive anal intercourse for 72 hours before and for 1 week after rectal biopsy procedure
- Willing to answer sexual behavior questions
- Cohort 1, Cisgender Males
- Assigned male sex at birth, currently identify as male gender (i.e. cisgender), man who has sex with men aged 18-59 years
- Able to provide informed consent in the official language of the study site's country
- HIV negative
- Receptive anal intercourse with a person assigned male sex at birth at least once in lifetime
- No history of taking supplemental steroids including testosterone replacement therapy in the last 12 months
- Willing to undergo peripheral blood and rectal biopsy sampling
- Willing to abstain from receptive anal intercourse for 72 hours before and for 1 week after rectal biopsy procedure.
- Willing to answer sexual behavior questions.
- Cohort 2, Longitudinal study with TGWSM planning to initiate feminizing hormone therapy
- Assigned male sex at birth with plans to start feminizing hormone therapy
- Aged 18-59 years
- Able to provide informed consent in the official language of the study site's country
You may not qualify if…
- History of inflammatory bowel disease or other inflammatory, infiltrative, infectious or vascular condition involving the lower gastrointestinal tract that, in the judgment of the investigators, may be worsened by study procedures or may significantly distort the anatomy of the distal large bowel
- Significant laboratory abnormalities at baseline visit for rectal biopsies, including but not limited to:
- Hemoglobin (Hgb) ≤ 10 g/dL
- Partial thromboplastin time (PTT) > 1.5x upper limit of normal (ULN) or international normalised ratio (INR) > 1.5x ULN
- Platelet count <100,000
- Any known medical condition that, in the judgment of the investigators, increases the risk of local or systemic complications of endoscopic procedures or pelvic examination, including but not limited to:
- Uncontrolled or severe cardiac arrhythmia
- Recent major abdominal, cardiothoracic, or neurological surgery in the last 12 months
- History of uncontrolled bleeding diathesis
- History of colonic, rectal, or vaginal perforation, fistula, or malignancy
- History or evidence on clinical examination of ulcerative, suppurative, or proliferative lesions of the anorectal mucosa.
- Use of systemic (oral/IV) antibiotics within the 4 weeks prior to rectal mucosal sampling.
- Participants may be screened/enrolled who do not meet this criterion, but rectal mucosal sampling will be deferred for at least 4 weeks from last systemic antibiotic use.
- Continued need for, or use during the 14 days prior to enrollment, of the following medications:
- Aspirin or more than 4 doses of nonsteroidal anti-inflammatory drugs (NSAIDs)
- Warfarin, heparin (low-molecular weight or unfractionated), platelet aggregation inhibitors, or fibrinolytic agents
- Any form of rectally administered agent besides products (lubricants or douching) used for sexual intercourse
- Continued need for, or use during the 90 days prior to enrollment, of the following medications:
- Systemic immunomodulatory agents
- Supraphysiologic doses of steroids with the exception of short course steroids <7 days duration at the discretion of the investigator and feminizing hormone therapy as detailed in inclusion criteria
- Experimental medications, vaccines, or biologicals
- Any other clinical condition or prior therapy that, in the opinion of the investigator, would make the patient unsuitable for the study or unable to comply with the study requirements.
Where it is running
- Hope Clinic — Atlanta, Georgia, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.