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NCT00344279

Changes in HIV Viral Load in Patients Undergoing Treatment for Filariasis

Completed Last updated 2 July 2017
What this trial tests

trial in Filarial Infection in 1,000 participants. Completed in 31 January 2012.

Timeline
8 August 2005
31 January 2012

Quick facts

Lead sponsorNational Institute of Allergy and Infectious Diseases (NIAID)
StatusCompleted
Study typeOBSERVATIONAL
Enrollment1,000
Start date8 August 2005
Estimated completion31 January 2012
Sites3 locations across India

Conditions studied

Sponsor

National Institute of Allergy and Infectious Diseases (NIAID)

Who can join

18 and older, any sex, with Filarial Infection or HIV Infections. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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 patients influences the amount of HIV virus in the blood and the progression of HIV infection to AIDS. Filarial infections are common in Chennai, and it is important to understand whether treatment of filariasis affects the course of HIV disease. The information gained from this study could be used to modify treatments for people both with HIV and filarial infections. Patients 18 years of age and older who are receiving treatment for HIV infection at the Government Hospital HIV clinic or YRG-Care may be eligible for this study. Two groups of patients will be recruited - patients with both HIV and filarial infections, and patients who have HIV infection alone, without filariasis. Candidates are screened with a medical history and review of medical records, physical examination, and blood and stool tests. Women have a urine pregnancy test. Within one month of screening, all participants receive a single dose of diethylcarbamazine and albendazole, a drug regimen commonly used to treat filarial infection. Patients are followed closely for the first 2 weeks after treatment to check for side effects. They are then seen at 1, 3, 6 and 12 months after the treatment dose for a physical examination and blood test.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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