Study to Improve Partner Services for STD Prevention (NCT00207467) | Clinical Trial Compass
CompletedPhase 2
Study to Improve Partner Services for STD Prevention
United States1,500 participantsStarted 2001-12
Plain-language summary
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).
Who can participate
Age range16 Years – 44 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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
What they're measuring
1
Index patient report of partner taking medicine at 6-8 weeks