Clinical Trials Directory

Trials / Completed

CompletedNCT00207467

Study to Improve Partner Services for STD Prevention

Prospective Study for Cost-Effectiveness Strategies to Improve Partner Notification: Female Trichomonas and Male Urethritis Studies

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
1,500 (planned)
Sponsor
Centers for Disease Control and Prevention · Federal
Sex
All
Age
16 Years – 44 Years
Healthy volunteers
Not accepted

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).

Detailed description

For partner treatment, index women who were diagnosed with trichomonas vaginalis and index men who were diagnosed with urethritis were randomized to one of three study arms: Standard partner referral (PR) - index patients were instructed to tell their partners that they need to go to a clinic for STI evaluation and treatment. Booklet-enhanced partner referral (BEPR) - index patients were given a wallet-sized booklet containing 4 tear-out cards with information for the partner and treatment guidelines for the providers that would see the partners. The partners could then present this card at a clinic to help the clinician better treat them. If index patients had more than 4 partners, they were given additional booklets. Patient delivered partner treatment (PDPT) - index patients were given packages containing 2 gram metronidazole (for TV patients) or azithromycin 1 gram and cefixime 400 mg (for urethritis patients) for up to 4 identified sex partners. When cefixime was no longer available, ciprofloxacin 500 mg was used. These packages contained written instructions about how to take the medication, warnings about side effects and a nurse's pager number to call if there were any questions or if the partner encountered any problems. All medications were distributed in containers with childproof caps and the partner's initial and birthdates were written on the bottle. This was a requirement of the Louisiana State Pharmacy Board. Names were not documented on the index patient's study or medical records.

Conditions

Interventions

TypeNameDescription
BEHAVIORALPatient-delivered partner treatment
BEHAVIORALBooklet-enhanced partner referral

Timeline

Start date
2001-12-01
Completion
2004-12-01
First posted
2005-09-21
Last updated
2005-09-21

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00207467. Inclusion in this directory is not an endorsement.