Could your mouthwash fight gonorrhea? new study investigates
NCT ID NCT04966507
First seen Jun 27, 2026 · Last updated Jul 10, 2026 · Updated 2 times
Summary
This study tested whether using an antibacterial mouthwash every day could lower the chance of getting gonorrhea in the throat. Researchers recruited 89 HIV-positive and HIV-negative men at high risk. Participants gargled with either Listerine or a placebo mouthwash daily. The study looked at how well people stuck with the routine and whether the mouthwash reduced infections.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Listerine Antiseptic Mouthwash (active ingredients: eucalyptol, menthol, methyl salicylate, thymol)
- What this could lead to
- If it works, daily mouthwash could become a simple, low-cost way to help prevent throat gonorrhea infections.
- What could go wrong
- This is a small, early-phase trial with only 89 participants. The mouthwash may not reduce infections enough to be meaningful, and results may not apply to the general population.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
89 people
The number who actually took part.
- Started
-
Feb 2022
- Finished
-
Dec 2025
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 45 years
- Sex
-
Male participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
This study will only include participants recruited as part an NIH/NIDA funded study (U01 DA036267 PIs Gorbach and Shoptaw) - the mSTUDY. By design, half of the participants are HIV-positive and half are HIV-negative and other inclusion criteria for the mSTUDY are as follows: 1. At least 18 but not older than 45 years of age on day of consent 2. Identified biologically male at birth 3. Willing to return for follow-up study visits every 6 months as long as the study is ongoing and be available to return for all study visits, barring unforeseen circumstances 4. Willing and able to provide written informed consent to take part in the study 5. Willing and able to provide adequate information for locator purposes 6. STI testing at each study visit (with reporting and treatment referral when indicated) 7. Understands and agrees to local STI reporting requirements 8. If HIV-negative at screening, report unprotected anal intercourse with a male in the past 6 months Additional inclusion criteria specific to this study are: 9. Currently enrolled in mSTUDY 10. mSTUDY participants who have turned 45 since enrollment in mSTUDY continue to be eligible for inclusion in this study. 11. Previously diagnosed with pharyngeal gonorrhea (while an mSTUDY participant) Participants will be excluded from the study if: 1. Mouthwash use is contraindicated, for example because of allergies or those who may need to avoid the high alcohol content of mouthwash such as recovery alcoholics maintaining their sobriety 2. They are unwilling to stop use of their current mouthwash during the 24-week study period
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Los Angeles LGBT Center
Los Angeles, California, 90028, United States
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