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Study to Improve Partner Services for STD Prevention

NCT00207467 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 1500

Last updated 2005-09-21

No results posted yet for this study

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).

Conditions

  • Trichomonas Vaginalis
  • Urethritis

Interventions

BEHAVIORAL

Patient-delivered partner treatment

BEHAVIORAL

Booklet-enhanced partner referral

Sponsors & Collaborators

Principal Investigators

  • Patty Kissinger, PhD · Tulane University School of Public Health and Tropical Medicine

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
44 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-12-31
Completion
2004-12-31

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00207467 on ClinicalTrials.gov