Study to Improve Partner Services for STD Prevention
Trichomonas Vaginalis, Urethritis
About this trial
This is an interventional prevention trial for Trichomonas Vaginalis focused on measuring patient-delivered partner treatment, partner referral, sexually transmitted diseases
Eligibility Criteria
Inclusion Criteria: Woman attending Family Planning Clinic or men attending STD clinic Aged 16-44 (non-pregnant women) - positive InPouch for trichomonas, or (pregnant women) - positive wet mount or InPouch for Trichomonas vaginalis (men) a complaint of urethritis which is verified on examination Report having >= 1sex partners in past 60 days Not presumptively treated for trichomonas (women) or urethritis (men) Provide informed consent to be re-contacted by telephone or in person in 14-28 days for a follow-up interview and T vaginalis or CT/GC rescreening Exclusion Criteria: Men Prisoner Has taken cefixime or azithromycin in last two weeks Has previously participated in the study All female partners are pregnant and did not have male partners Women client has taken metronidazole in the last two weeks client has been in this study previously women who are asymptomatic and in their first trimester of pregnancy
Sites / Locations
- Delgado STD Clinic
- Orleans Women's Health Clinic