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临床试验/NCT02979704
NCT02979704Unknown2 期

Randomized. Open Label Trial of Comparison Between Rosuvastatin and Atorvastatin on Oxidative Stress, Inflammatory and Thrombogenic Biomarkers in Patients With Hyperlipidemia

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2016年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
90
试验地点
1
主要终点
Establishment of superiority between rosuvastatin and atorvastatin on reduction of MDA in patients with hyperlipidemia

研究概览

简要总结

This study will be conducted to assess the status of oxidative stress inflammation and thrombogenesis in patients with hyperlipidemia and to compare the antioxidative, anti-inflammatory and antithrombogenic effects of rosuvastatin and atorvastatin.

详细描述

Hyperlipidemia is the major risk factor for development of atherosclerosis which ultimately leads to cardiovascular disease (CVD), an important cause of mortality and morbidity worldwide. Atherosclerosis was previously considered as a lipid storage disease but now growing evidence indicates that increased oxidative stress, vascular inflammation and platelet activation play an important role in the initiation and progression of atherosclerosis. Among the hypolipidemic drugs, statins, 3-hydroxyl-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors, have proved to be very much effective. Therefore, statins are the most widely used hypolipidemic agents. Evidence shows that besides hypolipidemic action statins possess antioxidative, anti-inflammatory and antithrombogenic effects known as pleiotropic action which might play an important role in attenuating the atherosclerotic process. However, pleiotropic effect varies with different members of statins.

The present prospective interventional study would be conducted in the Department of Pharmacology, Department of Cardiology and Internal Medicine, BSMMU from March 2016 to August 2017. Total 90 cases will be selected according to inclusion and exclusion criteria. The cases will be subdivided into 2 groups: group A and B. Group A consisting of 45 patients who will receive rosuvastatin (5-10) mg orally once daily and Group B consisting of 45 patients who will receive atorvastatin (10-20) mg orally once daily for 08 weeks. Patient's blood sample will be collected to measure baseline lipid profile, malondialdehyde (MDA), erythrocytic glutathione (GSH), high sensitive C-reactive protein (hs-CRP), prothrombin time (PT), platelet count. After obtaining baseline data patients will be assigned to the respective group. Parameters of baseline will again be evaluated after 08 weeks of therapeutic intervention. Regularity of drug intake will be ensured over telephone, pill count, and from the patient's compliance sheet. Patient's data will be recorded in a predetermined data sheet. Patients will be informed about study, its merits and demerits in easy language and then informed consent will be taken.Therefore, the present study has been designed to compare the antioxidative, anti-inflammatory and antithrombogenic effects of rosuvastatin and atorvastatin in hyperlipidemic patients to establish the superiority of a particular statin, so that it will provide a better therapeutic option in order to prevent CVD related mortality and morbidity.

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
None

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Rosuvastatin

Active Comparator

Intervention: Tablet Rosuvastatin (5-10) mg orally once daily dose for 08 weeks.

干预措施: Rosuvastatin (Drug)

Atorvastatin

Active Comparator

Intervention: Tablet Atorvastatin (10-20) mg orally once daily dose for 08 weeks

干预措施: Atorvastatin (Drug)

结局指标

主要结局

Establishment of superiority between rosuvastatin and atorvastatin on reduction of MDA in patients with hyperlipidemia

时间窗: [0 weeks (baseline), 8 weeks (end)] [safety Issue: No]

Reduction of oxidative stress will be measured by changes in level of MDA in µmol/L

Establishment of superiority between rosuvastatin and atorvastatin on reduction of inflammation in patients with hyperlipidemia

时间窗: [0 weeks (baseline), 8 weeks (end)] [safety Issue: No]

Reduction of inflammation will be measured by change in level of hs-CRP in mg/L

Establishment of superiority between rosuvastatin and atorvastatin on reduction platelet count in patients with hyperlipidemia

时间窗: [0 weeks (baseline), 8 weeks (end)] [safety Issue: No]

Reduction of thrombogenesis will be measured by changes in level of platelet count in per L of blood

Establishment of superiority between rosuvastatin and atorvastatin on increase prothrombin time in patients with hyperlipidemia

时间窗: [0 weeks (baseline), 8 weeks (end)] [safety Issue: No]

Reduction of thrombogenesis will be measured by changes in level of prothrombin time in per sec

Establishment of superiority between rosuvastatin and atorvastatin on increase level of erythrocytic GSH in patients with hyperlipidemia

时间窗: [0 weeks (baseline), 8 weeks (end)] [safety Issue: No]

Reduction of oxidative stress will be measured by changes in level of erythrocytic GSH in mg/gm of Hb

次要结局

未报告次要终点

研究者

发起方
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
申办方类型
Other
责任方
Principal Investigator
主要研究者

Samia Haque Tonu

Dr. and MD resident

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh

研究点 (1)

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