search
Back to results

Periodical Presumptive Treatment for the Control of Gonococcal Infections Among Sex Workers

Primary Purpose

Neisseria Gonorrhoeae Infection, Chlamydia Trachomatis, HIV

Status
Completed
Phase
Phase 4
Locations
Benin
Study Type
Interventional
Intervention
Monthly antibiotic
Monthly placebo
Sponsored by
CHU de Quebec-Universite Laval
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Neisseria Gonorrhoeae Infection focused on measuring Female sex workers, West Africa, Presumptive treatment, Sexually transmitted infections

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Female sex worker (seater) from one of the selected clusters

Exclusion Criteria:

  • Allergy to study drugs
  • Pregnancy
  • Intention to leave the city within the next 3 months

Sites / Locations

  • Dispensaire des infections sexuellement transmissibles

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Sugar pill

Treatment arm

Arm Description

Outcomes

Primary Outcome Measures

Presence of gonococcal infection
Cervical samples for NG PCR will be collected at the clinic visit planned at months 3 (between 45-134 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Presence of gonococcal infection
Cervical samples for NG PCR will be collected at the clinic visit planned at months 6 (between 135-224 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Presence of gonococcal infection
Cervical samples for NG PCR will be collected at the clinic visit planned at months 9 (between 225-315 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.

Secondary Outcome Measures

Presence of chlamydia infection
Cervical samples for CT PCR will be collected at the clinic visit planned at months 3 (between 45-134 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Presence of chlamydia infection
Cervical samples for CT PCR will be collected at the clinic visit planned at months 6 (between 135-224 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Presence of chlamydia infection
Cervical samples for CT PCR will be collected at the clinic visit planned at months 9 (between 225-315 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.

Full Information

First Posted
February 14, 2011
Last Updated
February 12, 2013
Sponsor
CHU de Quebec-Universite Laval
Collaborators
Maisonneuve-Rosemont Hospital, Centre de recherche du Centre hospitalier universitaire de Sherbrooke, Ministry of Health, Benin
search

1. Study Identification

Unique Protocol Identification Number
NCT01329588
Brief Title
Periodical Presumptive Treatment for the Control of Gonococcal Infections Among Sex Workers
Official Title
Periodical Presumptive Treatment of Gonorrhoea in Female Sex Workers: Impact on Prevalence of the Disease in Sex Workers and Their Clients
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Completed
Study Start Date
March 2001 (undefined)
Primary Completion Date
April 2002 (Actual)
Study Completion Date
April 2002 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
CHU de Quebec-Universite Laval
Collaborators
Maisonneuve-Rosemont Hospital, Centre de recherche du Centre hospitalier universitaire de Sherbrooke, Ministry of Health, Benin

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In the early years of the HIV epidemic in Africa, female sex workers (FSWs) were identified as a high-prevalence, high-incidence, core group among whom the extraordinary prevalence of other sexually transmitted infections (STIs) facilitated transmission of the virus to their clients, who then infected low-risk women not involved in the sex trade. In resource-poor settings, control of Neisseria gonorrhoeae (NG) and Chlamydia trachomatis (CT) among FSWs is difficult. The purpose of this study is to determine whether periodical antibiotic treatment (PAT) is effective in controlling these infections among West African FSWs. The study is designed as a cluster-randomized double-blind placebo-controlled trial conducted in West Africa. The study population consists of "seaters" FSWs who work from their homes in well-defined areas. Clusters will be paired according to their size and demographic characteristics of FSWs and clients. Within each pair, one cluster will be randomly allocated to the intervention and the other to the placebo group. At enrollment, participants will be interviewed, a pelvic examination performed, cervical swabs obtained for NG and CT polymerase chain reaction (PCR), and current cervicitis or vaginitis managed syndromically. Blood specimens will be obtained for HIV testing. All participants will be given free condoms and counseled on risk reduction. Monthly follow-up will be conducted within FSW communities, alternating with clinic visits where cervical samples will be collected. Study drugs (azithromycin 1 g and ciprofloxacin 500 mg, and their identical placebos) will be distributed every month according to a predefined schedule: directly-observed intake of azithromycin at months 1, 4 and 7, and ciprofloxacin at months 2, 3, 5, 6, 8 and 9. Data will be analyzed with SAS. The investigators will assess the time trends in NG and CT prevalence separately in both study groups using χ2-for-trend.
Detailed Description
"Seaters" are older, more stable, better organized, and have a much higher prevalence of HIV infection than FSWs who roam the streets or part-time sex workers. These communities (from 3 to 114 FSWs per site) will be aggregated into 18 clusters (one cluster was composed of 1-10 FSW communities) based on geographical proximity. Over a one-year period, FSWs from these clusters presenting to dedicated clinics will be invited to participate. In addition, field workers will visit FSWs at home or at prostitution sites to provide information about the trial and seek participation. Clusters will be paired according to their size and demographic characteristics of FSWs and clients. Within each pair, one cluster will be randomly allocated to the intervention and the other to the placebo group using pre-coded envelopes. With an average of 35 FSWs per cluster, the required number of cluster pairs is estimated at 8.7 to detect a 50% reduction in NG prevalence, assuming a baseline prevalence of 25%, 80% power and 5% alpha error.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neisseria Gonorrhoeae Infection, Chlamydia Trachomatis, HIV
Keywords
Female sex workers, West Africa, Presumptive treatment, Sexually transmitted infections

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
636 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Sugar pill
Arm Type
Placebo Comparator
Arm Title
Treatment arm
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Monthly antibiotic
Other Intervention Name(s)
Zithromax and cipro
Intervention Description
Azithromycin 1g per os once at months 1, 4 and 7 Ciprofloxacin 500 mg per os once at months 2, 3, 5, 6, 8 and 9
Intervention Type
Drug
Intervention Name(s)
Monthly placebo
Intervention Description
Azithromycin placebo (sugar pill) per os once at months 1, 4 and 7 Ciprofloxacin placebo (sugar pill) per os once at months 2, 3, 5, 6, 8 and 9
Primary Outcome Measure Information:
Title
Presence of gonococcal infection
Description
Cervical samples for NG PCR will be collected at the clinic visit planned at months 3 (between 45-134 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Time Frame
3 months
Title
Presence of gonococcal infection
Description
Cervical samples for NG PCR will be collected at the clinic visit planned at months 6 (between 135-224 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Time Frame
6 months
Title
Presence of gonococcal infection
Description
Cervical samples for NG PCR will be collected at the clinic visit planned at months 9 (between 225-315 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Presence of chlamydia infection
Description
Cervical samples for CT PCR will be collected at the clinic visit planned at months 3 (between 45-134 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Time Frame
3 months
Title
Presence of chlamydia infection
Description
Cervical samples for CT PCR will be collected at the clinic visit planned at months 6 (between 135-224 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Time Frame
6 months
Title
Presence of chlamydia infection
Description
Cervical samples for CT PCR will be collected at the clinic visit planned at months 9 (between 225-315 days after enrolment). Time trend in gonorrhoea prevalence will be analysed.
Time Frame
9 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Female sex worker (seater) from one of the selected clusters Exclusion Criteria: Allergy to study drugs Pregnancy Intention to leave the city within the next 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michel Alary, MD, PhD
Organizational Affiliation
Centre de recherche, Centre hospitalier affilié universitaire de Québec
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dispensaire des infections sexuellement transmissibles
City
Cotonou
Country
Benin

12. IPD Sharing Statement

Citations:
PubMed Identifier
22421690
Citation
Labbe AC, Pepin J, Khonde N, Dzokoto A, Meda H, Asamoah-Adu C, Mayaud P, Mabey D, Demers E, Alary M. Periodical antibiotic treatment for the control of gonococcal and chlamydial infections among sex workers in Benin and Ghana: a cluster-randomized placebo-controlled trial. Sex Transm Dis. 2012 Apr;39(4):253-9. doi: 10.1097/OLQ.0b013e318244aaa0.
Results Reference
derived

Learn more about this trial

Periodical Presumptive Treatment for the Control of Gonococcal Infections Among Sex Workers

We'll reach out to this number within 24 hrs