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Feasibility of an Oral Intervention for Sexual Health in Transgender Men

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Contents

clinicaltrials.gov/study/NCT06470906
Is a
‌
Clinical study
0

Clinical Study attributes

NCT Number
NCT064709060
Health Conditions in Trial
‌
Vaginal disease
0
Trial Recruitment Size
300
Trial Sponsor
Columbia University
Columbia University
0
Trial Collaborator
‌
Callen-Lorde Community Health Center
0
Clinical Trial Start Date
2024
0
Primary Completion Date
2025
0
Study Completion Date
2025
0
Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Treatment0
Intervention Type
Dietary Supplement0
Interventional Trial Phase
Not Applicable0
Official Name
Testosterone Effects on Sexual Health in Transgender Men: Feasibility Study of an Oral Intervention0
Last Updated
June 24, 2024
0
Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
Quadruple0
Masked Party
Investigator0
Participant0
Care Provider0
Outcomes Assessor0

Other attributes

Intervention Treatment
Probiotic Group0
Placebo Group0
Study summary

Transgender men (TGM) have a high incidence of sexually transmitted infected (STIs), including HIV, HPV and bacterial N. gonorrhea and C. trachomatis. In addition, TGM who start testosterone therapy (TT) experience significant vaginal morbidity that causes vaginal dryness and pain, due to the estrogen-inhibiting effects of TT on vaginal epithelium. Vaginal dysbiosis is a known contributor of increased STI risk and vaginal symptoms. In a future study, the investigators are planning a randomized trial of a 6-month oral Lactobacillus probiotics intervention in TGM on TT at the Callen-Lorde Community Health Center (CLCHC), New York City to determine whether this intervention can improve vaginal health in TGM on TT. In this study, the investigators will conduct a pilot and feasibility study to precede the main trial. The investigators will randomize 30 TGM on TT to receive either the intervention (consisting of Lactobacillus acidophilus GLA-14 and Lactobacillus rhamnosus HN001) or placebo (maltodextrin) for 4 weeks, evaluating the intervention's impact on vaginal microbiota and clinical outcomes, as well as its feasibility, acceptability, and adherence. This study will take place at the CLCHC Brooklyn site, aiming to gain pilot data, address feasibility and acceptability, and plan for the main trial accordingly.

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