NCT01190072终止不适用
LIPID-LOWERING THERAPY FOR SECONDARY PREVENTION IN PATIENTS UNDERGOING ELECTIVE PERCUTANEOUS CORONARY INTERVENTION (PCI) A 10-week, Open-label, Non-interventional Study of Total Cholesterol/LDL-cholesterol Management in Real Life in Coronary Patients Hospitalised for Elective PCI
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- AstraZeneca
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Serum total cholesterol concentration
研究概览
简要总结
The purpose of the study is to follow the management of blood lipids in patients with planned percutaneous coronary intervention (widening of coronary vessels) in a period from 6 to 10 weeks after the intervention.
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
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or nonpregnant female
- •Coronary patient hospitalised for elective PCI
- •Hypercholesterolaemia defined as LDL-C ≥ 2 mmol/L
排除标准
- •Any chronic inflammatory condition
- •Chronic anti-inflammatory pharmacotherapy (except low-dose ASA)
结局指标
主要结局
Serum total cholesterol concentration
时间窗: Once during the time period between Week 6 and Week 10
Serum LDL cholesterol concentration
时间窗: Once during the time period between Week 6 and Week 10
次要结局
- Proportion of patients achieving LDL-C < 2 mmol/L(Once during the time period between Week 6 and Week 10)
- Proportion of patients achieving total cholesterol < 4 mmol/L(Once during the time period between Week 6 and Week 10)
- Change of hsCRP levels from baseline(Once during the time period between Week 6 and Week 10)
研究者
研究点 (1)
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