This phase IV open-label protocol will determine the changes in weight, body composition, resting energy expenditure (REE), viral load, and CD4 + T-cell counts in HIV-infected patients receiving AZT/3TC (Combivir) and a protease inhibitor or a non-nucleoside analog. Thirty patients will be studied at New England Medical Center Hospitals, in Boston. Outpatients either naive to antiretroviral therapy, or needing a change of their current regimen and with no ongoing opportunistic infections will be eligible. After signing informed consent, patients will have a baseline visit, and follow up visits every 2 months for 6 months. Medical history, physical examination, adherance, failure of therapy and/or in tolerance will be assessed, and measurements of weight, body composition by bioelectric impedance and dual x-rays absorptiometry, REE, and blood tests will be performed at each visit. The primary end-point analysis will be made at 6 months.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000054-39S3
Application #
6454225
Study Section
Project Start
1999-12-01
Project End
2001-02-28
Budget Start
Budget End
Support Year
39
Fiscal Year
2001
Total Cost
Indirect Cost
Name
Tufts University
Department
Type
DUNS #
City
Boston
State
MA
Country
United States
Zip Code
02111
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