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临床试验/NCT05072054
NCT05072054Unknown4 期

Comparison of Effects of Atorvastatin Versus Rosuvastatin Treatment on Cardiac Function and Inflammation in Patients With Chronic Heart Failure With Reduced Ejection Fraction: A Randomised, Double Blind Clinical Study

Post Graduate Institute of Medical Education and Research, Chandigarh1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2019年10月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
发起方
入组人数
80
试验地点
1
主要终点
To compare the effect of atorvastatin and rosuvastatin on LVEF

研究概览

简要总结

Statins have a protective effect in patients with established heart failure because of their lipid-lowering and pleiotropic effects. There is no randomized controlled trial comparing lipophilic versus hydrophilic statins in these patients (head to head comparison). The best evidence so far is from a meta-analysis in which the authors did an adjusted indirect comparison between lipophilic statins and rosuvastatin and found that lipophilic statins were associated with significantly lower incidence of all-cause mortality, cardiovascular mortality, and hospitalization for worsening heart failure compared to rosuvastatin (hydrophilic statin) among patients with heart failure. So, the investigators plan to conduct a randomized controlled trial comparing the effects of atorvastatin and rosuvastatin on cardiac function in patients with heart failure with reduced ejection fraction.

详细描述

HMG CoA reductase inhibitors or Statins have been widely used for primary prevention and secondary prevention of atherosclerotic cardiovascular disease. Also, the protective effect of statins has been observed in patients with established heart failure because of their lipid-lowering and pleiotropic effects.

Various randomized and non-randomized clinical trials have evaluated statins like Atorvastatin, Rosuvastatin, Simvastatin, Pitavastatin and reported improved clinical outcomes in patients with heart failure with reduced ejection fraction as well as heart failure with preserved ejection fraction. Similar benefits on improved cardiac function, reduced inflammation, and improved mortality have been seen in small randomized controlled trials (RCTs) with Atorvastatin. The two large RCTs - Controlled Rosuvastatin Multinational Study in Heart Failure (CORONA) and Gruppo Italiano per lo Studio della Sopravvivenza nell'Insufficienza cardiac (GISSI-HF) - which compared Rosuvastatin versus placebo, failed to show statistically significant benefits in mortality outcomes in heart failure patients compared to placebo, although CORONA trial did show a significant reduction in hospital admissions but not on mortality.

However, these two large trials only compared one statin i.e rosuvastatin versus placebo; which is a hydrophilic statin. Statin is not a uniform class of drugs. They differ in their pleiotropic effects based on lipophilic nature. There is evidence that lipophilic statins enter cells via passive diffusion and are widely distributed to various tissues including cardiac tissues where it exerts pleiotropic actions whereas uptake of hydrophilic statins is via carrier-mediated mechanisms and is restricted to the liver, thus reduced the capacity of non-lipid effects on extra-hepatic tissues.

Currently, there is no RCT comparing lipophilic statin versus hydrophilic statin (head to head comparison). The best evidence so far is from a meta-analysis which is an adjusted indirect comparison between lipophilic statins and rosuvastatin. They found that lipophilic statins were associated with a significantly lower incidence of all-cause mortality, cardiovascular mortality, and hospitalization for worsening heart failure compared to rosuvastatin (hydrophilic statin) among patients with heart failure. So, the investigators plan to conduct a randomized controlled trial comparing the effects of atorvastatin and rosuvastatin on cardiac function and inflammation in patients with heart failure with reduced ejection fraction.

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, Care Provider, Investigator)

盲法说明

Patients will be randomized to two arms in ratio 1:1 using computer-generated random list. Patients, investigator and care provider will be blinded to the treatment group.

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Either gender,18-65 years of age
  • Left ventricular ejection fraction <40% as assessed by 2D echocardiography
  • NYHA class II-III
  • CHF patients currently optimized on standard treatment for at least 1 month before enrolment and on an OPD basis treatment
  • Ready to give written informed consent
  • Willing to comply with the study protocol

排除标准

  • Known hypersensitivity to statins
  • NYHA class IV patient
  • Serum creatinine >3 mg/dl
  • Significant liver disease: SGOT/SGPT >3 times the upper limit of normal (ULN) or >2.5 times the ULN in symptomatic patients
  • Patient on an enzyme inducer or inhibitor currently
  • Any malignancy or patient on chemotherapeutic agents
  • Pregnant or lactating females
  • Patients who have participated in another trial within the past 3 months
  • Patient with uncontrolled diabetes mellitus (HbA1c >7 g%)/ uncontrolled hypertension (BP >140/90 mmHg despite in ≥3 antihypertensive drugs)
  • Patient with HIV/ HBV / HCV infection

研究组 & 干预措施

Atorvastatin arm

Experimental

Tablet Atorvastatin 40mg once daily at bed-time given for 6 months

干预措施: Atorvastatin Oral Tablet (Drug)

Rosuvastatin arm

Active Comparator

Tablet Rosuvastatin 20mg once daily at bed-time given for 6 months

干预措施: Rosuvastatin Oral Tablet (Drug)

结局指标

主要结局

To compare the effect of atorvastatin and rosuvastatin on LVEF

时间窗: Measurements at enrolment (baseline), 3 month and 6 months

Change from baseline in Left ventricular ejection fraction (LVEF) measured by 2D Echocardiography after atorvastatin or rosuvastatin treatment

To compare the effect of atorvastatin and rosuvastatin on NT-ProBNP

时间窗: Measurements at enrolment (baseline), 3 months and 6 months

Change from baseline in NT-ProBNP (cardiac marker) after atorvastatin or rosuvastatin treatment.

次要结局

  • To compare the effect of atorvastatin and rosuvastatin on hsCRP(Measurements at enrolment (baseline), 3 month and 6 months)
  • Compare incidence of adverse events and major adverse events including all-cause mortality, non-fatal MI, stroke in atorvastatin and rosuvastatin group.(Analysis at 6 months)
  • To compare the effect of atorvastatin and rosuvastatin on IL-6(Measurements at enrolment (baseline) and 6 months)
  • To compare the effect of atorvastatin and rosuvastatin on Minnesota living with heart failure questionnaire (MLHFQ)(Measurements at enrolment (baseline), 3 month and 6 months)
  • To compare the effect of atorvastatin and rosuvastatin on 6-minute walk test (6MWT)(Measurements at enrolment (baseline), 3 month and 6 months)
  • Compare incidence of hospitalization for worsening of heart failure at 6 months in atorvastatin and rosuvastatin group(Analysis at 6 months)

研究者

发起方
Post Graduate Institute of Medical Education and Research, Chandigarh
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ashish Kakkar

Associate Professor, Department of Pharmacology

Post Graduate Institute of Medical Education and Research, Chandigarh

研究点 (1)

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