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临床试验/NCT01306565
NCT01306565已完成不适用

Comparison Between Effect of High Dose and Low Dose of Atorvastatin in Reduction Level of CRP in Patients With Unstable Angina and NSTEMI (Non ST Elevation MI)

Hormozgan University of Medical Sciences1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2009年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
100
试验地点
1
主要终点
CRP reduction

研究概览

简要总结

The aim of this study is to compare the effect of high dose and low dose of Atorvastatin in reduction level of C-reactive protein (CRP) in patients with unstable angina and NSTEMI (Non ST Elevation MI) attending Shahid Mohammadi hospital in Bandar Abbas.

详细描述

This study compare the effect of 80mg atorvastatin followed by two 20mg daily atorvastatin with three 80mg daily atorvastatin in reduction of CRP in patients with unstable angina and NSTEMI (Non ST Elevation MI) attending Shahid Mohammadi hospital in Bandar Abbas in 2009.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients with unstable angina with chest discomfort at rest with normal EKG or St depression (at least 0.1mv) in two consecutive leads or new and deep T inversion (at least 0.2mv)

排除标准

  • Myocardial Infarction with ST elevation
  • Diabetes Mellitus
  • Previous statin use
  • Current infectious disease

研究组 & 干预措施

High dose atorvastatin

Active Comparator

Three 80mg daily doses of atorvastatin

干预措施: Low dose Atorvastatin (Drug)

Low dose Atorvastatin

Experimental

80mg atorvastatin followed by two 20mg daily atorvastatin

干预措施: High dose atorvastatin (Drug)

结局指标

主要结局

CRP reduction

时间窗: 72 hours

CRP reduction will be compared between two study groups

次要结局

  • Drug side effects(72 hours)

研究者

申办方类型
Other

研究点 (1)

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