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Episodic Acyclovir Therapy for Genital Ulcers

Primary Purpose

HIV Infections, Ulcer, Herpes Simplex

Status
Completed
Phase
Phase 2
Locations
South Africa
Study Type
Interventional
Intervention
Acyclovir
Sponsored by
Centers for Disease Control and Prevention
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring HSV2, genital ulcer, HIV, South Africa, Treatment, Acyclovir, Prevention

Eligibility Criteria

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

Inclusion Criteria: Males presenting at the primary health care clinic with a genital ulcer Age 18 years or older Willing and able to give informed consent Willing to be tested for HSV and HIV Willing and able to comply with the study protocol including follow-up visits Willing to accept therapy by chance Exclusion Criteria: Extensive ulceration Ulceration >1 month History of adverse reaction to acyclovir Taking suppressive therapy for genital herpes History of renal insufficiency or proteinuria

Sites / Locations

  • Eloff Street Clinic
  • Green Door, Alexandra Health Centre

Outcomes

Primary Outcome Measures

Ulcer healing

Secondary Outcome Measures

HIV viral load from genital ulcers
HIV viral load in semen

Full Information

First Posted
September 9, 2005
Last Updated
September 10, 2012
Sponsor
Centers for Disease Control and Prevention
Collaborators
London School of Hygiene and Tropical Medicine, National Institute for Communicable Diseases, South Africa
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1. Study Identification

Unique Protocol Identification Number
NCT00164424
Brief Title
Episodic Acyclovir Therapy for Genital Ulcers
Official Title
Impact of Episodic Acyclovir Therapy on Ulcer Duration and HIV Shedding From Genital Ulcers Among Men in South Africa
Study Type
Interventional

2. Study Status

Record Verification Date
September 2012
Overall Recruitment Status
Completed
Study Start Date
March 2005 (undefined)
Primary Completion Date
March 2009 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centers for Disease Control and Prevention
Collaborators
London School of Hygiene and Tropical Medicine, National Institute for Communicable Diseases, South Africa

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to determine if acyclovir episodic treatment has an effect in ulcer healing and if it should be added to the syndromic management of genital ulcer disease.
Detailed Description
Background and Objectives: Herpes simplex virus type 2 (HSV-2) is the primary cause of genital ulcer and one of the most prevalent sexually transmitted infections (STI) worldwide. HSV-2 has been recognized as a risk factor for HIV in multiple studies. A substantial shift in the aetiology of genital ulcer disease (GUD) towards genital herpes has been noted in many countries in Africa, especially those with mature HIV epidemics. Some countries guided by the predominance of HSV-2 as the aetiology of GUD in their country, are changing syndromic guidelines to include acyclovir as part of the treatment for GUD. Little data is available to support this decision in terms of its effect on clinical course and its cost-effectiveness. Yet, substantial investment would be needed in poor countries to add acyclovir to their essential drug list. Studies to determine the appropriateness of episodic acyclovir therapy for HSV-2 in the developing world are needed. Episodic therapy with acyclovir both as a treatment modality and as an HIV-prevention strategy is appealing, in terms of cost and sustainability. However, it is not clear which will be its impact under field conditions in which there would be delay in symptom recognition and treatment initiation, and whether these conditions could be optimized through patient education. We propose to conduct a randomized placebo-controlled trial of the effect of HSV-2 episodic therapy on symptomatic herpes and on HIV shedding from genital ulcers. This study will help answer the question if acyclovir therapy for herpes should be added into the syndromic management of genital ulcer disease. Acyclovir has an acceptable profile for widespread STI treatment and is now relatively inexpensive and well-tolerated. Given that HSV-2 is the leading cause of GUD in the developing world, this approach could have great public health importance, by providing a safe, acceptable, and cost-effective method to treat genital ulcer disease and potentially reduce HIV transmission. If acyclovir therapy reduces HIV shedding, its incorporation into syndromic management would provide and effective way to scale it up as a public health intervention. Methods: We plan an individually randomized double blind placebo-control trial of the WHO and US CDC recommended dose of 3-times daily acyclovir for a 5-day treatment course. The trial will be conducted at two primary health care clinics in Johannesburg, South Africa. A total of 600 men presenting to the clinic with GUD will be enrolled in the study. Consenting participants will be randomized to receive either acyclovir plus syndromic management or placebo plus syndromic management. Syndromic management for genital ulcer disease will consist of one dose antibiotics to cover for syphilis and chancroid. Participants will be followed for a month; during follow-up visits duration of ulcers, ulcer number and size will be evaluated and ulcer, blood and semen samples collected to test for HIV RNA viral loads among HIV-positives and for HSV-2 shedding. Timeline: Duration of the project is 2 years Expected Outcomes: The main outcome of the study will be the evaluation of the impact of acyclovir therapy on ulcer healing. We will also measure the impact of acyclovir therapy on HIV and HSV-2 viral load from genital ulcers and HIV viral load in semen.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Ulcer, Herpes Simplex
Keywords
HSV2, genital ulcer, HIV, South Africa, Treatment, Acyclovir, Prevention

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
Double
Allocation
Randomized
Enrollment
613 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Acyclovir
Primary Outcome Measure Information:
Title
Ulcer healing
Secondary Outcome Measure Information:
Title
HIV viral load from genital ulcers
Title
HIV viral load in semen

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Males presenting at the primary health care clinic with a genital ulcer Age 18 years or older Willing and able to give informed consent Willing to be tested for HSV and HIV Willing and able to comply with the study protocol including follow-up visits Willing to accept therapy by chance Exclusion Criteria: Extensive ulceration Ulceration >1 month History of adverse reaction to acyclovir Taking suppressive therapy for genital herpes History of renal insufficiency or proteinuria
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gabriela Paz Bailey, MD
Organizational Affiliation
Centers for Disease Control and Prevention
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
David Lewis, MD
Organizational Affiliation
STIRC, National Institute for Communicable Diseases (NICD), South Africa
Official's Role
Principal Investigator
Facility Information:
Facility Name
Eloff Street Clinic
City
Johannesburg
State/Province
Gauteng
Country
South Africa
Facility Name
Green Door, Alexandra Health Centre
City
Johannesburg
State/Province
Gauteng
Country
South Africa

12. IPD Sharing Statement

Citations:
PubMed Identifier
20443734
Citation
Paz Bailey G, Sternberg M, Lewis DA, Puren A. Acute HIV infections among men with genital ulcer disease in South Africa. J Infect Dis. 2010 Jun 15;201(12):1811-5. doi: 10.1086/652785.
Results Reference
derived
PubMed Identifier
19715417
Citation
Paz-Bailey G, Sternberg M, Puren AJ, Markowitz LE, Ballard R, Delany S, Hawkes S, Nwanyanwu O, Ryan C, Lewis DA. Improvement in healing and reduction in HIV shedding with episodic acyclovir therapy as part of syndromic management among men: a randomized, controlled trial. J Infect Dis. 2009 Oct 1;200(7):1039-49. doi: 10.1086/605647.
Results Reference
derived

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Episodic Acyclovir Therapy for Genital Ulcers

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