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STI Care Model to Reduce Genital Inflammation and HIV Risk in South African Women

Primary Purpose

HIV Prevention, Sexually Transmitted Diseases

Status
Completed
Phase
Not Applicable
Locations
South Africa
Study Type
Interventional
Intervention
Point-of-care STI testing
Sponsored by
Centre for the AIDS Programme of Research in South Africa
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for HIV Prevention focused on measuring point-of-care testing, sexually transmitted infections, expedited partner therapy, genital inflammation

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 18 - 40 years
  • Female gender
  • HIV negative antibody test at enrollment

Exclusion Criteria:

  • HIV positive women
  • Pregnant women
  • Women who have had antibiotic treatment within the last 7 days
  • Women who disclose any form of sex work

Sites / Locations

  • CAPRISA

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Diagnostic STI care

Arm Description

All participants underwent point-of-care STI testing, and if diagnosed with a STI were offered immediate therapy, and expedited therapy if indicated.

Outcomes

Primary Outcome Measures

Changes in genital inflammation in women diagnosed with STIs after a diagnostic care intervention
Genital cytokine measurements before and after the intervention

Secondary Outcome Measures

Prevalence of laboratory-diagnosed STIs in women presenting to the Prince Cyril Zulu Communicable Diseases Clinic, Durban, South Africa
Prevalence of chlamydia, gonorrhoea and trichomoniasis in young women presenting for syndromic STI care
Validation of GeneXpert technology for STI testing against laboratory-based STI assays
GeneXpert validation
Acceptability of implementing expedited partner therapy among patients
Proportion of patients taking up expedited partner therapy

Full Information

First Posted
January 9, 2018
Last Updated
January 24, 2018
Sponsor
Centre for the AIDS Programme of Research in South Africa
Collaborators
Johns Hopkins University, National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT03407586
Brief Title
STI Care Model to Reduce Genital Inflammation and HIV Risk in South African Women
Official Title
Changing the STI Care Model to Reduce Genital Inflammation and HIV Risk in South African Women
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
May 15, 2016 (Actual)
Primary Completion Date
February 1, 2017 (Actual)
Study Completion Date
February 1, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Centre for the AIDS Programme of Research in South Africa
Collaborators
Johns Hopkins University, National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this prospective cohort study is to determine if a model of care including point-of-care testing, immediate therapy, expedited partner therapy and test of cure will result in a higher cure rate and a lower recurrence rate of sexually transmitted infections (STIs), with a subsequent reduction in genital inflammatory cytokines and hence HIV risk among young women in a high burden setting in KwaZulu-Natal, South Africa. The study will identify individuals with STIs using the GeneXpert system for the simultaneous detection of Neisseria gonorrhoeae and Chlamydia trachomatis, and Trichomonas vaginalis. Genital tract cytokines will be measured using Bio-Plex Pro Human Cytokine kits and a Bio-Plex MagPix Array Reader. Following point-of-care diagnosis, participants will be treated immediately with appropriate therapy under direct supervision, offering the participants expedited partner therapy for their partners. STI testing and cytokine assessments will be repeated after 6 and 12 weeks, to determine if these have decreased. Overall, this study will provide some evidence on whether this STI care model can have an impact on STI prevalence and genital tract inflammation, in a low- and middle-income country, where currently syndromic STI management is the standard of care.
Detailed Description
Sexually transmitted infections (STIs) are strongly associated with HIV risk. However, population based studies to manage STIs as a way of reducing HIV risk have had limited success. Recent studies show that elevated genital tract inflammatory cytokines are strongly associated with an increased risk of HIV acquisition, and STIs are one of the commonest causes of elevated genital tract cytokines. This interest in the role of cytokines in HIV acquisition has reinvigorated interest in STIs and whether better management strategies can have a role to play in HIV risk reduction. HIV and STIs are extremely common in the South African province of KwaZulu-Natal, where there are many challenges with STI diagnosis and treatment, including the reliance on syndromic management, an approach based on the recognition of STI syndromes (vaginal discharge, urethral discharge and genital ulceration), followed by treatment targeting the common causes of the syndrome. This syndromic management approach has a low sensitivity and specificity for detecting the most common curable STIs, such as chlamydia, gonorrhoea, trichomoniasis and syphilis. Studies have shown that only 13% of symptomatic STI infections are cured with the STI treatment services currently offered in KwaZulu-Natal. This low cure rate for symptomatic STIs is compounded by the fact that up to 80% of STIs are asymptomatic, which results in a majority of STIs remaining undiagnosed and untreated. Other challenges with current STI management include limited partner notification and treatment, resulting in high levels of reinfection. At a population level, the result is that most STIs remain untreated and the burden of STIs within the community remains unchecked. The goal of the study is to determine if an innovative, enhanced programme of STI management will result in a higher cure rate and a lower recurrence rate, with a subsequent reduction in genital inflammatory cytokines and hence HIV risk. This proof-of-concept cohort study will identify individuals with STIs using an innovative, point-of-care diagnostic test, an automated, cartridge-based nucleic amplification assay (GeneXpert) for the simultaneous detection of Neisseria gonorrhoeae and Chlamydia trachomatis, and Trichomonas vaginalis. This technology has been introduced on a large scale across South Africa to detect tuberculosis (TB) and TB drug resistance, thereby accelerating diagnosis, treatment and enhancing public health initiatives to control TB. Genital tract cytokines will be measured using Bio-Plex Pro Human Cytokine kits and a Bio-Plex MagPix Array Reader. Following point-of-care diagnosis, participants will be treated immediately with appropriate therapy under direct supervision, giving the participants the same treatment to take home for their sexual partners (expedited partner therapy) and asking them to return after six weeks and three months for a test of cure and additional cytokine assessments, to determine if these have decreased. Overall, this innovative enhanced management package for targeted STI care, offers the best opportunity to reduce STIs, by ensuring that the individual is cured and by reducing the risk of reinfection using expedited partner therapy. This will allow the investigators to determine whether genital inflammation can be reduced after effective targeted STI treatment, and ultimately reduce the risk of HIV acquisition in South Africa.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Prevention, Sexually Transmitted Diseases
Keywords
point-of-care testing, sexually transmitted infections, expedited partner therapy, genital inflammation

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Prospective cohort study
Masking
None (Open Label)
Masking Description
All participants provided written informed consent to join the intervention of diagnostic rather than syndromic management.
Allocation
N/A
Enrollment
267 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Diagnostic STI care
Arm Type
Other
Arm Description
All participants underwent point-of-care STI testing, and if diagnosed with a STI were offered immediate therapy, and expedited therapy if indicated.
Intervention Type
Diagnostic Test
Intervention Name(s)
Point-of-care STI testing
Intervention Description
All participants underwent point-of-care STI testing (GeneXpert), and if diagnosed with a STI were offered immediate therapy, and expedited therapy, if indicated.
Primary Outcome Measure Information:
Title
Changes in genital inflammation in women diagnosed with STIs after a diagnostic care intervention
Description
Genital cytokine measurements before and after the intervention
Time Frame
Baseline and 6 and 12 weeks after the intervention
Secondary Outcome Measure Information:
Title
Prevalence of laboratory-diagnosed STIs in women presenting to the Prince Cyril Zulu Communicable Diseases Clinic, Durban, South Africa
Description
Prevalence of chlamydia, gonorrhoea and trichomoniasis in young women presenting for syndromic STI care
Time Frame
Baseline
Title
Validation of GeneXpert technology for STI testing against laboratory-based STI assays
Description
GeneXpert validation
Time Frame
Baseline
Title
Acceptability of implementing expedited partner therapy among patients
Description
Proportion of patients taking up expedited partner therapy
Time Frame
6 weeks and 3 months after intervention

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18 - 40 years Female gender HIV negative antibody test at enrollment Exclusion Criteria: HIV positive women Pregnant women Women who have had antibiotic treatment within the last 7 days Women who disclose any form of sex work
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nigel J Garrett, MBBS
Organizational Affiliation
Centre for the AIDS Programme of Research in South Africa
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Anne Rompalo, MD
Organizational Affiliation
Johns Hopkins University
Official's Role
Principal Investigator
Facility Information:
Facility Name
CAPRISA
City
Durban
State/Province
KwaZulu-Natal
ZIP/Postal Code
4001
Country
South Africa

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Data will be published in open access journal together with manuscript, and will thereby be shared with other researchers.
IPD Sharing Time Frame
The manuscript and supporting information are currently under review at PLOS ONE journal and are expected to be published indefinitely by 31 January 2018.
Citations:
PubMed Identifier
30782948
Citation
Garrett N, Mitchev N, Osman F, Naidoo J, Dorward J, Singh R, Ngobese H, Rompalo A, Mlisana K, Mindel A. Diagnostic accuracy of the Xpert CT/NG and OSOM Trichomonas Rapid assays for point-of-care STI testing among young women in South Africa: a cross-sectional study. BMJ Open. 2019 Feb 19;9(2):e026888. doi: 10.1136/bmjopen-2018-026888.
Results Reference
derived

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STI Care Model to Reduce Genital Inflammation and HIV Risk in South African Women

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