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Recruiting Phase 2 NCT07088419

"Sexual Health Assessment of TinidaZole Against M. Genitalium (SHAZAM)"

Trial Parameters

Condition Mycoplasma Genitalium
Sponsor University of Washington
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 40
Sex MALE
Min Age 18 Years
Max Age N/A
Start Date 2025-07-23
Completion 2026-08-01
Interventions
Tinidazole

Brief Summary

The objective is to estimate the efficacy of tinidazole for the treatment of Mycoplasma genitalium (MG) among male patients who have been diagnosed with non-gonococcal urethritis (NGU) at the Public Health - Seattle \&King County (PHSKC) Sexual Health Clinic (SHC). Tinidazole was approved by the Food and Drug Administration (FDA) in May 2004 to treat other infections (i.e., trichomoniasis, giardiasis, amebiasis, bacterial vaginosis) but has not been systematically tested for effectiveness against M. genitalium. The dosing that the investigators are proposing does not significantly increase the risk associated with taking tinidazole and this investigation meets criteria for an IND exemption.

Eligibility Criteria

Inclusion Criteria: * ≥18 years of age * Clinical diagnosis of NGU * Urogenital MG documented by a positive NAAT in the prior 7 days * Fluent in English * Assigned male at birth * Attending the PHSKC SHC * Able to provide informed consent * Able to undergo a test of cure (TOC) 21 days after completing the tinidazole regimen Exclusion Criteria: * Known allergy to tinidazole * Other contraindications to tinidazole * At the clinician's discretion

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