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A Study to Compare Anti-HIV Drugs Given Twice a Day or Once a Day, With or Without Direct Observation

Phase 2
Completed
Conditions
HIV Infections
Registration Number
NCT00036452
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Brief Summary

Anti-HIV drug therapy works best when the drugs are taken exactly as prescribed by a doctor. Because anti-HIV therapy often involves multiple drugs, some people have difficulty taking them all correctly. The easier it is to take anti-HIV drugs, the more likely people will take them as prescribed and get the best results. This study will see if people are more successful in taking anti-HIV drugs once a day or twice a day. It also will determine if having a health care professional oversee each weekday dose helps people control their HIV infection. The study will compare taking a three-drug combination twice a day versus taking a three-drug combination just once a day. The study will also compare patients taking the drugs on their own to patients taking the drugs in the presence of a clinical worker. Viral load (amount of HIV in the blood) and drug side effects will be measured.

Detailed Description

While many factors contribute to the success or failure of antiretroviral therapy for HIV, among the most important are factors that influence adherence to a treatment regimen, such as duration of therapy, dosing frequency, pill burden, side effects, and patient behaviors. Inconsistent adherence or nonadherence to antiretroviral therapy can result in suboptimal drug exposure. Suboptimal drug exposure can, in turn, impact short- and long-term patient outcomes by increasing the likelihood of drug resistant HIV mutants and subsequent virologic and clinical failure. It is therefore essential to design treatment regimens that promote long-term adherence to potent antiretroviral therapy. This study will evaluate the relative contribution of reduced-frequency dosing and directly observed therapy on the magnitude and durability of virologic suppression in patients treated with potent antiretroviral therapy.

Patients will be randomly assigned to one of three study arms. Arms A, B, and C receive the same daily dosage of lopinavir/ritonavir (LPV/r), emtricitabine (FTC), and stavudine extended release (d4T XR) or tenofovir DF (TDF). In Arm A, drugs are self-administered for 48 weeks; LPV/r is taken twice daily and FTC and d4T XR or TDF once daily. In Arm B, all drugs are self-administered once daily for 48 weeks. In Arm C, drugs are taken once a day under directly observed therapy during Weeks 0-24, and then by self-administration during Weeks 25-48. Adherence to the regimen is measured using an electronic drug monitoring system. Viral load, CD4 and CD8 T cell responses, population pharmacokinetics, and quality of life indicators are measured throughout the study. The tolerability and safety of the treatment regimens are also monitored.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
402
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (29)

The Ohio State Univ. AIDS CRS

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Columbus, Ohio, United States

MetroHealth CRS

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Cleveland, Ohio, United States

Pitt CRS

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Pittsburgh, Pennsylvania, United States

University of Colorado Hospital CRS

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Aurora, Colorado, United States

Ucsd, Avrc Crs

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San Diego, California, United States

NY Univ. HIV/AIDS CRS

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New York, New York, United States

Johns Hopkins Adult AIDS CRS

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Baltimore, Maryland, United States

Hosp. of the Univ. of Pennsylvania CRS

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Philadelphia, Pennsylvania, United States

University of Washington AIDS CRS

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Seattle, Washington, United States

USC CRS

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Los Angeles, California, United States

Univ. of California Davis Med. Ctr., ACTU

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Sacramento, California, United States

Indiana Univ. School of Medicine, Infectious Disease Research Clinic

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Indianapolis, Indiana, United States

Univ. of Miami AIDS CRS

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Miami, Florida, United States

Univ. of Hawaii at Manoa, Leahi Hosp.

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Honolulu, Hawaii, United States

IHV Baltimore Treatment CRS

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Baltimore, Maryland, United States

SSTAR, Family Healthcare Ctr.

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Fall River, Massachusetts, United States

Beth Israel Med. Ctr., ACTU

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New York, New York, United States

McCree McCuller Wellness Ctr. at the Connection, Infectious Disease Unit

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Rochester, New York, United States

AIDS Care CRS

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Rochester, New York, United States

Univ. of Rochester ACTG CRS

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Rochester, New York, United States

Regional Center for Infectious Disease, Wendover Medical Center CRS

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Greensboro, North Carolina, United States

Unc Aids Crs

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Chapel Hill, North Carolina, United States

Univ. of Cincinnati CRS

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Cincinnati, Ohio, United States

Wake County Health and Human Services CRS

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Raleigh, North Carolina, United States

Wits HIV CRS

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Johannesburg, Gauteng, South Africa

Vanderbilt Therapeutics CRS

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Nashville, Tennessee, United States

Puerto Rico-AIDS CRS

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San Juan, Puerto Rico

The Miriam Hosp. ACTG CRS

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Providence, Rhode Island, United States

University of Minnesota, ACTU

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Minneapolis, Minnesota, United States

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