MedPath

A Comparison of Two Tests for Anti-HIV Drug Resistance

Completed
Conditions
HIV Infections
Registration Number
NCT00006490
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Brief Summary

The purpose of this study is to compare 2 different types of tests of the HIV virus to see which specific anti-HIV drugs would work the best.

Drug resistance is a major reason for therapy failure in HIV patients. Two types of tests can detect resistance to drugs: 1) genotyping (sequencing), which looks at the DNA sequence of a virus to see whether it has developed any genetic resistance; 2) phenotyping, which looks at the ability of different drugs to suppress virus growth in the laboratory. Genotyping and phenotyping can help doctors give patients the most effective drug therapy.

Detailed Description

The emergence of drug resistance is a major factor contributing to the failure of antiretroviral therapy in HIV-infected patients. Drug resistance can be detected by genotypic or phenotypic assays, both having distinct advantages and disadvantages. Results from genotypic and phenotypic testing are helpful in excluding from the subsequent regimen drugs to which the resistance is identified, and both tests predict virologic response to salvage therapy in patients who have failed a previous regimen. Resistance testing is likely to be beneficial as an aid in selecting a salvage regimen.

At entry, patients are randomized to Arm A (sequencing) or Arm B (phenotyping) and have a resistance test drawn while still receiving the current regimen even though regimen failure is suspected. The test results are available between Weeks 1 and 4, inclusive. There are weekly visits for the first 4 weeks after entry to monitor viral load and maintenance of the current failing (prestudy) regimen. If virologic failure is confirmed, a new regimen is chosen and prescribed at the first visit after resistance test results are available. \[AS PER AMENDMENT 12/6/00: If the resistance assay fails to yield results, another regimen is chosen and prescribed based on the patient's medical and medication history.\] If virologic failure is not confirmed, the current drug regimen is not changed. Otherwise, on-site study visits occur every 4 weeks until Week 24 and then every 8 weeks thereafter through Week 48. \[AS PER AMENDMENT 12/6/00: on-site study visits occur every 4 weeks until Week 24 and then every 8 weeks thereafter\]. Medical resource use is assessed at baseline and then every 8 weeks through Week 48. Quality of life is assessed at baseline and then every 16 weeks through Week 48.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
600
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (47)

Univ of Miami School of Medicine

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Miami, Florida, United States

Harvard (Massachusetts Gen Hosp)

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Boston, Massachusetts, United States

The CORE Ctr

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Chicago, Illinois, United States

Beth Israel Deaconess - West Campus

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Boston, Massachusetts, United States

Moses H Cone Memorial Hosp

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Greensboro, North Carolina, United States

Univ of Cincinnati

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Cincinnati, Ohio, United States

Case Western Reserve Univ

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Cleveland, Ohio, United States

MetroHealth Med Ctr

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Cleveland, Ohio, United States

Ohio State Univ Hosp Clinic

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Columbus, Ohio, United States

Philadelphia Veterans Administration Med Ctr

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Philadelphia, Pennsylvania, United States

Univ of Pennsylvania

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Philadelphia, Pennsylvania, United States

Univ of Texas, Southwestern Med Ctr of Dallas

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Dallas, Texas, United States

Univ of Washington

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Seattle, Washington, United States

Univ of Alabama at Birmingham

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Birmingham, Alabama, United States

Bellevue Hosp / New York Univ Med Ctr

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New York, New York, United States

Univ of Hawaii

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Honolulu, Hawaii, United States

Emory Univ

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Atlanta, Georgia, United States

Northwestern Univ Med School

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Chicago, Illinois, United States

UCLA CARE Ctr

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Los Angeles, California, United States

Denver Dept of Health and Hosps

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Denver, Colorado, United States

Harbor UCLA Med Ctr

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Torrance, California, United States

Santa Clara Valley Med Ctr / AIDS Community Rsch Consortium

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San Jose, California, United States

Cornell Univ Med Ctr

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New York, New York, United States

University of California San Francisco

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San Francisco, California, United States

Univ of Southern California / LA County USC Med Ctr

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Los Angeles, California, United States

Johns Hopkins Hosp

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Baltimore, Maryland, United States

Beth Israel Med Ctr

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New York, New York, United States

Columbia Presbyterian Med Ctr

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New York, New York, United States

Stanford Univ Med Ctr

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Stanford, California, United States

Univ of California San Francisco

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San Francisco, California, United States

San Mateo AIDS Program / Stanford Univ

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Stanford, California, United States

Rush Presbyterian - Saint Luke's Med Ctr

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Chicago, Illinois, United States

Univ of Colorado Health Sciences Ctr

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Denver, Colorado, United States

Brigham and Women's Hosp

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Boston, Massachusetts, United States

SUNY / Erie County Med Ctr at Buffalo

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Buffalo, New York, United States

Carolinas Med Ctr

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Charlotte, North Carolina, United States

Duke Univ Med Ctr

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Durham, North Carolina, United States

Univ of Pittsburgh

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Pittsburgh, Pennsylvania, United States

Miriam Hosp / Brown Univ

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Providence, Rhode Island, United States

Willow Clinic

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Menlo Park, California, United States

Cornell Clinical Trials Unit - Chelsea Clinic

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New York, New York, United States

Univ of North Carolina

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Chapel Hill, North Carolina, United States

Mount Sinai Med Ctr

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New York, New York, United States

Brown Univ / Miriam Hosp

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Providence, Rhode Island, United States

Univ of Puerto Rico

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San Juan, Puerto Rico

Vanderbilt Univ Med Ctr

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Nashville, Tennessee, United States

Julio Arroyo

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West Columbia, South Carolina, United States

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