NCT01867203撤回不适用
Lipid-lowering Therapy Individualization
Cliniques universitaires Saint-Luc- Université Catholique de Louvain1 个研究点 分布在 1 个国家开始时间: 2017年8月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 发起方
- 试验地点
- 1
- 主要终点
- Cholesterol levels-side effects
研究概览
简要总结
Patients needing lipid lowering therapy will be recruited before initiation of the treatment. For each patient, total and LDL cholesterol levels before start of therapy will be measured. One, three and six months after his/her first visit, when steady-state will be reached, for each included patient, the cholesterol levels will be re-assessed in order to evaluate the response to statin therapy calculated as the amplitude of cholesterol reduction. The aim is to assess the association between patient's genotype and the response to statin therapy.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 25 Years 至 80 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient known to be compliant
- •Age [25-80]
- •treated with Atorvastatin, simvastatin, fluvastatin.
排除标准
- •Pregnancy
结局指标
主要结局
Cholesterol levels-side effects
时间窗: 1 to 6 months
次要结局
未报告次要终点
研究者
研究点 (1)
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