Study to Improve Partner Services for STD Prevention

Completed · Phase 2

Conditions studied: Trichomonas Vaginalis, Urethritis

In brief

The goal of this study was to examine the efficacy of patient-delivered partner treatment (PDPT) compared to standard partner referral (PR) and booklet enhanced partner referral (BEPR).

Key facts

Study ID

NCT00207467

Run by

Centers for Disease Control and Prevention

People needed

1500

Starts

2001-12-01

Expected to finish

2004-12-01

Last updated by the study team

2005-09-21

Who can join

Age: 16 and older, up to 44. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Delgado STD Clinic — New Orleans, Louisiana, United States
• Orleans Women's Health Clinic — New Orleans, Louisiana, United States

Full record on ClinicalTrials.gov

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