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Completed

NCT Number: NCT00107887

TB (Tuberculosis) Preventive Therapy for HIV Patients With Access to HAART (Highly Active Antiretroviral Therapy)

The purpose of this study is to determine if implementing a policy of widespread INH (Isoniazid) prophylaxis therapy in HIV-infected patients with access to antiretroviral therapy reduces the incidence of active TB disease in the HIV clinic population.

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Key information

About this study

Tuberculosis remains a major public health problem in Brazil. Approximately 35% of HIV-infected adults in Rio de Janeiro are co-infected with latent TB. The Brazilian policies for the provision of treatment to HIV-infected people are among the most progressive in the world. Brazil provides combination antiretroviral therapy free of charge to all patients who meet clinical criteria and maintains an extensive clinic and laboratory system for the appropriate prescription and monitoring of therapy. The use of IPT, however, has been very limited in Brazil and TB remains a prominent disease in AIDS patients.

A clustered randomized trial (CRT) will determine if the routine detection of latent TB in HIV-infected patients identified at HIV clinics in Rio de Janeiro, followed by treatment with isoniazid, will reduce TB incidence in this population. The CRT will take a phased-implementation approach to ensure that all clinics will eventually have full coverage.

This study will determine if implementing a policy of widespread IPT use in HIV-infected patients with access to ARV therapy reduces the incidence of active TB disease in the HIV clinic population. The study population will be comprised of HIV-infected individuals who attend any of the 29 government HIV clinics in Rio de Janeiro, Brazil. We expect that IPT use in addition to ARVs will result in a 40-60% reduction in TB incidence, and that approximately 50% of the prevented TB cases will be in patients not yet eligible for HAART.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Attending 1 of 29 participating HIV clinics
  • Confirmed HIV infection
  • Age > 15 years

Exclusion criteria

  • Current active TB disease
  • TB infection within 2 years
  • Hepatitis

Treatment and study plan

INH preventive therapy

Drug

Clinics will receive training regarding the use of IPT for prevention of Tuberculosis

TST (tuberculin skin test)

Drug

Clinics will be trained in the use of TST for assessing exposure to TB

Primary outcomes

  1. Measured incidence of active TB in HIV clinic population before and following implementation of IPT policy

    Time frame: 6 Years

  2. Comparative impact of IPT (Isoniazid Preventive Therapy) and ARVs (antiretrovirals) on TB incidence in the HIV clinic population

    Time frame: 6 Years

Secondary outcomes

  1. Characteristics of TST+ vs. TST+ HIV-infected patients

    Time frame: 6 Years

  2. Clinical, demographic and laboratory predictors of developing active TB

    Time frame: 6 Years

  3. Lessons learned related to training and implementation

    Time frame: 6 Years

Sponsors and collaborators

Lead sponsor

Johns Hopkins University

Other

Collaborators

  • Bill and Melinda Gates Foundation
  • Communicable Disease Program, Brazil
  • Consortium to Respond Effectively to the AIDS/Tuberculosis Epidemic

Registry information

Official study title

Impact of TB Preventive Therapy for HIV/TB Co-infected Patients With Access to Highly Active Antiretroviral Therapy in Rio de Janeiro, Brazil: A Phased Implementation Trial

Important dates

Study start
2005
Primary completion
2010
Study completion
2010
First posted
Apr 12, 2005
Registry last updated
Jun 15, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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