NCT01164397已完成不适用
Efficiency of Rosuvastatin Versus the Fixed Combination of Ezetimibe/Simvastatin to Reduce the Cholesterol Levels in Outpatients in a Realistic Environment. A Retrospective Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 268
- 试验地点
- 1
- 主要终点
- The percentage of the patients that achieve the goal proposed for NCEP ATP III (2001 y 2004) will be assessed, to C-LDL in patients treated with Rosuvastatin or Ezetimibe/Simvastatin at least for 8 weeks.
研究概览
简要总结
The aim of this study is to evaluate the effectiveness of Rosuvastatin versus Ezetimibe/Simvastatin in dyslipidemic patients treated for at least 8 weeks.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Retrospective
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Dislipidemic population treated with rosuvastatin or ezetimibe/simvastatin for at least for 8 weeks
- •Who have completed at least 80% of the treatment
- •To have determinations at least of CT, TG C-LDL and CHDL before starting treatment and after 8 weeks of taking the medicine
排除标准
- •Initiating different therapy lipid lowering to Rosuvastatin or Ezetimibe/Simvastatin
结局指标
主要结局
The percentage of the patients that achieve the goal proposed for NCEP ATP III (2001 y 2004) will be assessed, to C-LDL in patients treated with Rosuvastatin or Ezetimibe/Simvastatin at least for 8 weeks.
时间窗: Data will be collected using CRFs after complete at least 15 patients over a 24 week period.
次要结局
- The percentage of LDL-C reduction according to baseline levels in patients treated wuth Rosuvastatin or Ezetimibe/Simvastatin for at least 8 weeks.(Data will be collected using CRFs after complete at least 15 patients over a 24 week period.)
研究者
研究点 (1)
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