Effect of Atazanavir on Endothelial Function in HIV-Infected Patients Compared to Standard Proteinase Inhibitors on Top of Potent Antiviral Combination Therapy
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 2
- 主要终点
- Change of flow-mediated dilation in the forearm after 6 months using the protease inhibitor atazanavir in a potent antiviral therapy combination compared with a combination including current proteinase inhibitor.
研究概览
简要总结
It is known that certain antiviral therapies, the socalled protease inhibitors, used in the treatment of HIV infection has an untowarded effect on the blood vessels, promoting early occurence of atherosclerosis. A a newer protease inhibitor, atazanavir, has been shown to have no negative effect on the levels of blood cholesterol and it is hypothesized that this may indicate that atazanavir is less prone to induce atherosclerosis. An early sign of atherosclerosis is a reduced vasomotion and this study investigate the influence of atazanavir on functionality of the conduit blood vessels compared to that of "standard" antiviral therapy.
详细描述
Indication: Dyslipidemia Type II in HIV-Infected Patients
Primary Objectives: Change of flow-mediated dilation in the forearm after 6 months using the protease inhibitor atazanavir in a potent antiviral therapy combination compared with a combination including current proteinase inhibitor.
Secondary Objectives: Changes in plasma lipid profiles and further clinical chemistry parameters after 6 months of treatment compared to baseline.
Study Design: This is a multicenter, observer-blind (measurements of vessel parameters and statistical evaluation), treatment-controlled, randomized, study with 2 treatment groups.
Planned Total Sample Size: (40-50) eligible randomized patients (20-25 per group) from 2-5 centers.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Single
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men and women, 18 to 65 years old.
- •HIV-infection, documented by HIV-antibody ELISA and either positive immunoblot for HIV-antibodies or presence of HIV1 in blood.
- •Two consecutive Roche Ultrasensitive Amplicor tests showing plasma HIV-1 RNA < 50 copies/ml within 60 days prior to study entry.
- •CD4 count of > 100 cells/ml during 60 days prior to study entry.
- •Stable antiretroviral therapy for at least 12 weeks prior to study entry (a protease inhibitor plus 2 NRTIs).
- •Patient's treatment history allows, in the opinion of the investigator, atazanavir as replacement for current PI, i.e. continued viral suppression is expected based upon patient's treatment history and results of previous resistance testing, if available.
- •Fasting LDL-cholesterol > 3.0 mmol/l.
排除标准
- •Known coronary artery disease, hypertension, peripheral artery disease, or cerebrovascular disease.
- •Diabetes mellitus.
- •Serious illness requiring systemic treatment and/or hospitalization within 14 days prior to study entry.
- •Any contraindication for study medication.
- •Currently on non-nucleoside reverse transcriptase inhibitors (NNRTI) (previous exposure allowed).
- •Previous virologic failure on proteinase inhibitor-containing regimens which was not the consequence of poor adherence to therapy or drug adverse events; i.e. virologic failure was probably due to lack of potency of drug regimen, and may consecutively have resulted in protease resistance mutations.
- •Previously documented protease resistance mutations which are known to result in cross-resistance against atazanavir.
- •Any lipid lowering drugs within 4 weeks prior to study entry.
- •Testosterone or anabolic steroids unless stable therapy at least 12 weeks prior to study entry.
- •Systemic glucocorticoids, long-acting inhaled steroids or other immunomodulators within 30 days prior to study entry (prednisone < 10mg/day or equivalent is permitted.
- •Drug or alcohol abuse, in the opinion of the investigator rendering the patient unreliable for participation.
- •Participation in any other drug/treatment study.
结局指标
主要结局
Change of flow-mediated dilation in the forearm after 6 months using the protease inhibitor atazanavir in a potent antiviral therapy combination compared with a combination including current proteinase inhibitor.
次要结局
- Changes in plasma lipid profiles and further clinical chemistry parameters after 6 months of treatment compared to baseline.