The study is designed to evaluate the proportion of patients with tenofovir induced proteinuria that will resolve their proteinuria when the tenofovir containing nucleoside/nucleotide backbone is switched to a raltegravir backbone. Common HIV treatment regimens contain nucleoside/nucleotide combinations that may have long-term side effects including nephrotoxicity. Switching these backbones out for an integrase inhibitor based regimen has not been systematically evaluated. Hypothesis: Proteinuria developing during treatment with tenofovir improves or resolves when tenofovir is switched out with raltegravir. Switching to a nuc- sparing regimen, containing raltegravir and a boosted protease inhibitor in patients without preexisting protease inhibitor mutations is safe and does not lead to virologic failure
As described in the brief summary, this is a pilot study to evaluate for improvements in proteinuria when switched off from Tenofovir
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Change of the tenofovir based nucleoside part of the HIV regimen to raltegravir, 400mg BID
Patients With Reduced or Resolved Proteinuria
Measurement of Protein in Urine samples at end of study visit
Time frame: 24 weeks
Patients Without HIV Re-bound
HIV Viral load blood test at week 24
Time frame: 24 weeks
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