跳至主要内容
临床试验/NCT06053983
NCT06053983已完成4 期

Comparison Between Atorvastatin and Rosuvastatin in Reduction of Inflammatory Biomarkers in Patients With Acute Coronary Syndrome

Rawalpindi Medical College1 个研究点 分布在 1 个国家目标入组 126 人开始时间: 2023年1月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
126
试验地点
1
主要终点
Mean Change C-reactive protein

研究概览

简要总结

This study will help us to compare atorvastatin and rosuvastatin in terms of their ability to reduce biomarkers of inflammation in patients of acute coronary syndrome

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
Double (Participant, Investigator)

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

  • Patients with age 18 years and above, of both genders, diagnosed with acute coronary syndrome (as per operational definition) who were not taking statins previously.
  • Patients who sign written informed consent to participate in the study.

排除标准

  • 1.Patients who are taking either statins and/or any other drug which lower serum lipid levels, patients with a history of statin hypersensitivity, patients in whom statins are contraindicated.
  • 2.Patients who will be surgically managed will be also excluded. 3.if coronary revascularization will be planned or anticipated at the time of screening.
  • 4.Pregnant or lactating women. 5.Patients having concomitant infections which cause the rise of inflammatory markers.

研究组 & 干预措施

rosuvastatin 20 mg

Experimental

干预措施: Turbox CRP kit (Device)

rosuvastatin 20 mg

Experimental

干预措施: rosuvastatin 20 mg, (Drug)

atorvastatin 40 mg

Experimental

干预措施: Turbox CRP kit (Device)

atorvastatin 40 mg

Experimental

干预措施: atorvastatin 40 mg (Drug)

结局指标

主要结局

Mean Change C-reactive protein

时间窗: AFTER 4 WEEKS

hs -CRP (mg/l)

次要结局

未报告次要终点

研究者

发起方
Rawalpindi Medical College
申办方类型
Other
责任方
Principal Investigator
主要研究者

Naima Shehzadi Qazi

Dr. NAIMA SHEHZADI QAZI PGT MD CARDIOLOGY

Rawalpindi Medical College

研究点 (1)

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