Collecting data on maintaining anti-retroviral activity (quantitative HIV RNA determination) and immunological activity (CD4 cells) after switching from protease inhibitor or NNRTI to Nevirapine (Viramune®) and collecting of routinely observed laboratory data on lipids, and liver enzymes.
Study Type
OBSERVATIONAL
Enrollment
55
Change in viral load (HIV-RNA)
Time frame: Baseline, up to 52 weeks
Change in CD4 cell count
Time frame: Baseline, up to 52 weeks
Change in lipid parameters
mg/dl
Time frame: Baseline, up to 52 weeks
Change in glucose
mg/dl
Time frame: Baseline, up to 52 weeks
Assessment of subjective well-being
verbal rating scale
Time frame: up to 52 weeks
Assessment of tolerability by physician and patients
verbal rating scale
Time frame: after 52 weeks
Change in liver enzyme parameter
U/l
Time frame: Baseline, up to 52 weeks
Number of patients with adverse events
Time frame: up to 52 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.