Three Generic Nevirapine-Based Antiretroviral Treatments in Chinese Patients:Multicentric Observation Cohort
Phase 4
Completed
- Conditions
- HIV Infections
- Interventions
- Registration Number
- NCT00618176
- Lead Sponsor
- Peking Union Medical College
- Brief Summary
The purpose of this study is to determine whether the three generic nevirapine-based antiretroviral regimens are effective in the treatment of Acquired immune deficiency syndrome .
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 198
Inclusion Criteria
- 18 years or older
- the subjects were HIV-seropositive by standard serum enzyme-linked immunosorbent assay (ELISA) tests and also by Western blot analysis
- the subjects were antiretroviral drug-naïve
- a baseline CD4+ T-cell count from 100 to 350 cells/mm3 and a baseline plasma viral load over 500copies/ml
Exclusion Criteria
- pregnancy or breastfeeding
- anticipated nonadherence
- AIDS-defining illness within 2 weeks of entry
- white blood cell count less than 2.0×109/L, absolute neutrophil count less than 1.0×109/L, hemoglobin level less than 90g/l, platelet count less than 0.75×1012/L
- transaminase and alkaline phosphatase level more than 3 times the upper limit of the normal range, bilirubin level more than 2.5times the upper limit of the normal range, serum creatinine level more than 1.5 times the upper limit of the normal range
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description B Stavudine (d4T), Lamivudine (3TC), Nevirapine (NVP) - A Zidovudine (AZT)+ Didanosine (ddI)+ Nevirapine (NVP) - C Zidovudine (AZT), Lamivudine (3TC), Nevirapine (NVP) -
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Peking Union Medical College Hospital
🇨🇳Beijing, China