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UnknownNCT03412071

Effect of Antibiotics on Penile Microbiome and HIV Susceptibility Study in Ugandan Men

Testing the Ability of a Microbiome - Focused Intervention to Reduce HIV Susceptibility in Ugandan Men

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
125 (estimated)
Sponsor
University of Toronto · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This pilot study will assess the impact of four antimicrobial products (3 topical, one systemic) on the foreskin microbiome and HIV susceptibility of foreskin-derived CD4+ T cells. Participants will include HIV-uninfected Ugandan men presenting for elective male circumcision to reduce their HIV risk.

Detailed description

RATIONALE: The foreskin is the site of most HIV acquisition in uncircumcised heterosexual men, and male circumcision (MC) reduces HIV risk by almost 60%. However, cultural and practical barriers have led to suboptimal uptake. Foreskin inflammation, defined by elevated levels of pro-inflammatory cytokines in the prepuce, is a key determinant of HIV acquisition risk in uncircumcised men, and anaerobic bacteria within the foreskin microbiome may be an important cause of this inflammation. OBJECTIVES: A pilot in vivo - in vitro clinical study of four potential interventions to reduce HIV susceptibility in the foreskin by altering the microbiome. The study is a collaboration between the University of Toronto, IAVI-UVRI, and the Entebbe General Hospital. We will recruit 125 men presenting for elective MC, along with regular female sexual partners (if applicable). Participants will be randomized (n=25 per group) to immediate MC, or to one of four intervention arms: twice-daily application of topical metronidazole 0.75%; twice-daily application of topical clindamycin 2%; twice daily application of hydrogen peroxide 1%; or oral tinidazole 2g once a day for two days. Swabs for immune and microbiome studies will be collected before and after product. After 4 weeks the MC procedure will be performed; foreskin CD4+ T cell susceptibility to HIV will be quantified using a flow cytometry-based pseudovirus assay, and tissue immunohistochemistry performed. The primary and secondary endpoints are outlined below. A secondary study will assess the impact of penile topical antibiotic application on immunology and the microbiome in the genital tract of female sexual partners. OUTCOMES: This in vivo - in vitro clinical trial will define the causal role of the penile microbiome in HIV susceptibility, and will assess potential strategies to take forward into HIV efficacy trials in uncircumcised heterosexual men.

Conditions

Interventions

TypeNameDescription
DRUGOral TinidazolePlease see description under arms
DRUGTopical metronidazolePlease see description under arms
DRUGTopical ClindamycinPlease see description under arms
DRUGTopical Hydrogen PeroxidePlease see description under arms

Timeline

Start date
2017-12-07
Primary completion
2019-12-07
Completion
2019-12-07
First posted
2018-01-26
Last updated
2018-01-26

Locations

1 site across 1 country: Uganda

Source: ClinicalTrials.gov record NCT03412071. Inclusion in this directory is not an endorsement.