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Completed

NCT Number: NCT00106171

Anti-HIV Medications for People Recently Infected With HIV

It is not known if anti-HIV treatment for recently infected patients improves long-term patient prognosis. The purpose of this study is to determine if a one year course of anti-HIV medications slows progression of HIV disease in adults recently infected with HIV.

Study hypothesis: A one-year course of HAART administered during acute or early seroconversion may slow the progression of HIV infection.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

University of British Columbia, Vancouver, British Columbia, Canada

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About this study

Although some doctors favor starting anti-HIV treatment as soon as possible after patients learn they are infected, it is not known if treatment for recently infected patients results in slower progression of HIV disease. This study will compare the virologic outcomes of recently infected adults who receive highly active antiretroviral therapy (HAART) with those who receive no treatment. This study will also compare the effects of treatment on patients who enroll within 3 months of seroconversion (acute seroconverters) with patients who enroll within 3 to 12 months of seroconversion (early seroconverters).

This study will last at least 3 years. Participants will be randomly assigned to one of two groups. Group 1 will receive HAART for 1 year; Group 2 will receive no treatment. There will be at least 20 study visits over the 3-year study period. Blood collection will occur at all study visits. A physical exam, medical and medication history, and risk behavior assessment will occur at most visits; participants will also be asked to complete an adherence questionnaire at most visits.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Documented acute or recent HIV infection (infected in the past 12 months) as defined in the study protocol
  • Antiretroviral naive. Participants who have taken antiretrovirals for postexposure prophylaxis are eligible for this study.
  • Able to swallow tablets or capsules
  • Willing to use acceptable forms of contraception

Exclusion criteria

  • Physician unable to design a potentially effective HAART regimen based on results of genotypic resistance testing
  • Two CD4 counts of less than 350 cells/mm3 obtained at least 7 days apart within 30 days of study entry
  • Viral load less than 5,000 copies/ml within 30 days of study entry in participants who have been infected with HIV-1 for more than six months prior to study entry
  • Use of systemic cancer chemotherapy, systemic investigational agents, specific antiretroviral medications, or immunomodulators (growth factors, systemic corticosteroids, HIV vaccines, immune globulin, interleukins, interferons) within 30 days prior to study entry
  • Current alcohol or drug use that, in the opinion of the investigator, would interfere with the study
  • Serious illness requiring systemic treatment or hospitalization until participant either completes therapy or is clinically stable on therapy for at least 7 days prior to study entry
  • Currently involuntarily incarcerated for treatment of either a psychiatric or physical (e.g., infectious disease) illness
  • Pregnancy or breastfeeding

Treatment and study plan

highly active antiretroviral therapy (HAART)

Drug

Regimens will be assigned by investigators

Primary outcomes

  1. Total Treatment-free Time to Initiation of Permanent HAART

    Time frame: Through study completion, an average of 18 months

    All HAART-free time from initial infection with HIV to initiation of permanent HAART

Secondary outcomes

  1. Toxicity as Assessed by the of Number of Participants With Serious Adverse Events

    Time frame: Throughout study completion, an average of 18 months

    Number of participants with serious adverse events (grade 3 or 4 as defined by the NIH toxicity scale)

Sponsors and collaborators

Lead sponsor

Johns Hopkins Bloomberg School of Public Health

Other

Collaborators

  • National Institute of Allergy and Infectious Diseases (NIAID)

Registry information

Official study title

A Randomized Trial of HAART in Acute/Early HIV Infection

Important dates

Study start
2005
Primary completion
2012
Study completion
2012
First posted
Mar 22, 2005
Registry last updated
Sep 13, 2023

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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