Clinical Trials Directory

Trials / Completed

CompletedNCT03671239

Rectal Microbicide Acceptability, Tolerability and Adherence

Acceptability, Tolerability, and Adherence of Three Rectal Microbicide Placebo Formulations Among HIV Seronegative Cisgender Men, Transgender Men and Transgender Women Who Engage in Receptive Anal Intercourse

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
217 (actual)
Sponsor
Microbicide Trials Network · Network
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

MTN-035 is a multi-site, randomized-sequence, three-period, open label crossover study that will enroll approximately 210 participants randomized (1:1:1:1:1:1) to one of six sequences of rectal microbicide placebo product application.

Detailed description

MTN-035 is a multi-site, randomized-sequence, three-period, open label crossover study that will enroll approximately 210 participants randomized (1:1:1:1:1:1) to one of six sequences of rectal microbicide placebo product application. At the start of each 4-week product use period, participants will receive either rectal inserts, rectal douches, or rectal suppositories and be instructed to use their assigned study product prior to each receptive anal intercourse (RAI) encounter during that period. Participants who do not have RAI in a given week will be asked to use the product without sex. There will be a 1-week washout period between each of the three product use periods. Participant follow-up will take approximately 3.5 months.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPlacebo rectal insertParticipants will be instructed to insert in the rectum a placebo insert prior to RAI. If a dose is missed, participants will be instructed to wait to take a dose at the next occurrence of RAI. Furthermore, if no RAI activity occurs at all in a given 7-day period, participants will be instructed to take a dose on the seventh day in the absence of RAI.
BEHAVIORALPlacebo rectal suppositoryParticipants will be instructed to insert in the rectum a placebo suppository prior to RAI. If a dose is missed, participants will be instructed to wait to take a dose at the next occurrence of RAI. Furthermore, if no RAI activity occurs at all in a given 7-day period, participants will be instructed to take a dose on the seventh day in the absence of RAI.
BEHAVIORALPlacebo rectal doucheParticipants will be instructed to insert in the rectum a placebo douche (enema bottle with approximately 120 mL of clean tap water or bottled water) prior to RAI. If a dose is missed, participants will be instructed to wait to take a dose at the next occurrence of RAI, or if no other RAI activity occurs in that 7-day period, to take a dose in the absence of RAI. Furthermore, if no RAI activity occurs at all in a given 7-day period, participants will be instructed to take a dose on the seventh day in the absence of RAI.

Timeline

Start date
2019-04-26
Primary completion
2020-07-27
Completion
2020-07-27
First posted
2018-09-14
Last updated
2023-01-20
Results posted
2023-01-20

Locations

7 sites across 5 countries: United States, Malawi, Peru, South Africa, Thailand

Source: ClinicalTrials.gov record NCT03671239. Inclusion in this directory is not an endorsement.