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临床试验/NCT02930265
NCT02930265Unknown不适用

Chinese People's Liberation Army General Hospital

Chinese PLA General Hospital1 个研究点 分布在 1 个国家目标入组 400 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
不适用
发起方
入组人数
400
试验地点
1
主要终点
main adverse cardiovascular events

研究概览

简要总结

It has been known that liraglutide reduces infarct size, improved left ventricular function, reduce myocardial stunning, and play a protective role in myocardial ischemia-reperfusion injury for patients with acute myocardial infarction. But it is not sure whether liraglutide can benefit patients with ischemic cardiomyopathy. This study aim to explore the effect of Liraglutide in improving cardiac function for patients with ischemic cardiomyopathy.

详细描述

Investigators will enroll 400 patients with ischemic cardiomyopathy who were admitted to the Chinese PLA General Hospital. All patients enrolled in this study will collect detailed baseline clinical data, including blood, enzymes (troponin, creatine kinase), blood sugar, serum creatinine, blood lipid levels (LDL lipoprotein cholesterol, high density lipoprotein cholesterol, triglycerides, total cholesterol), brain natriuretic peptide (BNP), inflammatory markers (high sensitivity C- reactive protein, interleukin-6), endothelin (ET-1), pancreas glucagon-like peptide -1 (GLP-1) and superoxide dismutase (SOD).

The investigators randomly assign eligible patients in a 1:1 ratio to either liraglutide intervention group (N = 200) or control group (N = 200), liraglutide intervention group will accept ischemic cardiomyopathy conventional drugs and liraglutide (Novo Nordisk, specifications: 18mg / 3ml; 1.8mg subcutaneous injection of 1 / day), Control group will accept ischemic cardiomyopathy conventional drugs and a placebo.

Primary end point of the study is main adverse cardiovascular events including Recurrent myocardial infarction, recurrent angina, revascularization, all-cause death, nonfatal myocardial infarction, nonfatal stroke, hospitalization for heart failure again. Secondary end point of the study was 1) New York Heart Association functional class, 2) left ventricular ejection fraction, 3) 6-minute walk test, 4) KCCQ clinical total score, 5) changes in blood glucose levels during follow-up, blood lipid levels and body weight

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

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 Ischemic Cardiomyopathy: The clinical manifestations of heart failure (NYHA class II-IV grade), evidence of cardiac dysfunction (LVEF ≤40%, and LVEDD ≥55mm) and previous coronary angiography showed one or more severe coronary artery stenosis.

排除标准

  • Valvular heart disease
  • dilated cardiomyopathy
  • patients requiring emergency PCI
  • patients with cardiogenic shock;
  • there have been recent acute myocardial infarction in one month;
  • there have been recent acute stroke in one month;
  • estimated glomerular filtration over rate eGFR <30ml / min / 1.73m2 (according to MDRD formula);
  • malignant tumor
  • severe liver failure
  • respiratory failure

研究组 & 干预措施

Liraglutide intervention group

Active Comparator

Liraglutide intervention group will accept ischemic cardiomyopathy conventional drugs and Liraglutide (Novo Nordisk, specifications: 18mg / 3ml; 1.8mg subcutaneous injection of 1 / day)

干预措施: Liraglutide (Drug)

结局指标

主要结局

main adverse cardiovascular events

时间窗: Followed up for 6 months after enrolled in the study

Primary end point of the study is main adverse cardiovascular events including Recurrent myocardial infarction, recurrent angina, revascularization, all-cause death, nonfatal myocardial infarction, nonfatal stroke, hospitalization for heart failure again

次要结局

  • New York Heart Association functional class(Followed up for 6 months after enrolled in the study)
  • left ventricular ejection fraction(Followed up for 6 months after enrolled in the study)
  • 6-minute walk test(Followed up for 6 months after enrolled in the study)
  • KCCQ (Kansas City cardiomyopathy questionnaire) clinical total score(Followed up for 6 months after enrolled in the study)

研究者

发起方
Chinese PLA General Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Qian geng

Associate attending doctor

Chinese PLA General Hospital

研究点 (1)

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