Status:

COMPLETED

Changes in HIV Viral Load in Patients Undergoing Treatment for Filariasis

Lead Sponsor:

National Institute of Allergy and Infectious Diseases (NIAID)

Conditions:

Filarial Infection

HIV Infections

Eligibility:

All Genders

18+ years

Brief Summary

This study, sponsored by the National Institutes of Health and the Tuberculosis Research Centre and YRG-Care in Chennai, India, will examine how treatment of lymphatic filariasis in HIV-infected patie...

Detailed Description

To determine the effect of pre-existing filarial infection and its treatment on viral burden and clinical parameters in patients infected with HIV, this study aims to follow plasma HIV loads, CD4 coun...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Greater than 18 years of age.
  • Ability to give informed consent
  • HIV positive
  • If on antiretrovirals or treatment for opportunistic infections, have it be a stable maintenance period of at least 2 months
  • Male or female, providing women are neither pregnant nor breast-feeding
  • Willingness to adhere to the testing schedule of the protocol and to provide small amounts of blood (5 ml) on multiple occasions
  • Willingness to be treated with DEC/albendazole
  • Willingness, if female, to be tested for pregnancy and to be informed of the test result
  • Willingness to have samples stored for future research
  • EXCLUSION CRITERIA:
  • Acutely ill at the time of enrollment into the study i.e. newly diagnosed with an opportunistic infection and not yet stabilized on a treatment regime.
  • Hemoglobin less than 9 g/l for women and less than 10 g/l for men
  • AST, ALT greater than 5 times normal
  • Evidence of acute HIV infection (acute antiretroviral syndrome)
  • Active tuberculosis or known tuberculosis
  • A true allergy to DEC or albendazole
  • At the discretion of the investigator if it is felt that someone is not appropriate for the study (i.e. known active drug use, patient with history of chronic noncompliance in clinic visits)

Exclusion

    Key Trial Info

    Start Date :

    August 8 2005

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    January 31 2012

    Estimated Enrollment :

    1000 Patients enrolled

    Trial Details

    Trial ID

    NCT00344279

    Start Date

    August 8 2005

    End Date

    January 31 2012

    Last Update

    July 2 2017

    Active Locations (3)

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    Page 1 of 1 (3 locations)

    1

    Government General Hospital

    Chennai, India

    2

    Tuberculosis Research Centre

    Chennai, India

    3

    YRG Care

    Chennai, India