跳至主要内容
临床试验/NCT02737319
NCT02737319已完成4 期

A Randomized Trial of Rosuvastatin in Elective Percutaneous Coronary Intervention to Prevent Contrast-induced (CLEAR-CIN).

University of Sao Paulo1 个研究点 分布在 1 个国家目标入组 493 人开始时间: 2011年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
493
试验地点
1
主要终点
Contrast induce nephropathy defined by serum creatinine increase more than 0.3mg/dl or 50% higher than baseline

研究概览

简要总结

The investigators analyzed the HMG-CoA reductase inhibitor, rosuvastatin, for the prevention of contrast-medium-induced nephropathy in patients undergoing primary angioplasty.

详细描述

Patients with stable coronary artery disease already taking chronic statin undergoing elective angioplasty are at risk for contrast-medium-induced nephropathy because there are specified risk factors as age more than 75 years, chronic renal insufficiency, diabetes, use of contrast and the lack of effective prophylaxis.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • chronic statin use
  • positive stress test findings (electrocardiography, nuclear imaging, or stress echocardiography
  • elective angioplasty.

排除标准

  • non-statin therapy
  • any presentation of ACS within 24 hours before the time of randomization
  • current use of potent CYP3A4 inhibitors, including azole antifungals, protease inhibitors, macrolide antibiotics, and cyclosporine
  • renal replacement therapy, a history of kidney transplant, pregnant and with renal failure (serum creatinine > 3.0 mg/dl).

研究组 & 干预措施

Rosuvastatin

Experimental

40 mg of Rosuvastatin up to 6 hours before elective percutaneous coronary intervention.

干预措施: Rosuvastatin (Drug)

结局指标

主要结局

Contrast induce nephropathy defined by serum creatinine increase more than 0.3mg/dl or 50% higher than baseline

时间窗: 48 hours

Serum creatinine increase more than 0.3mg/dl or 50% higher than baseline

次要结局

  • Composite end-point ( all cause of death; acute renal failure and no-fatal mayocardial infarctio.(48 hours)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kleber Bomfim Araujo Martins

MD,PhD

University of Sao Paulo

研究点 (1)

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