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临床试验/NCT03083119
NCT03083119Unknown2 期

The Methylation Regulation Mechanism of Blood Stasis Relevant miRNA Expression on Coronary Heart Disease

Jie Wang1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2017年3月20日最近更新:
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
70
试验地点
1
主要终点
major adverse cardiovascular events

研究概览

简要总结

In this study, typical cases of coronary heart disease are selected. They will be intervened by Xuesaitong soft capsules to investigate efficacy and safety for Coronary Heart disease.

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

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

入选标准

  • Clinical diagnosis of coronary angiography unstable angina
  • Clinical diagnosis of unstable angina
  • Age of 30 to 75 years old
  • Not use thrombolysis, dilate coronary drugs within two weeks
  • Sign the consent

排除标准

  • Severe valvular heart disease
  • Insulin-dependent diabetes
  • mental disease
  • Combined with severe liver, kidney, hematopoietic system disorder
  • Patients with malignant tumors
  • Pregnancy or breast-feeding women
  • Recent history of trauma
  • Drug allergy

研究组 & 干预措施

Xuesaitong soft capsule group

Experimental

Patients who confirmed by coronary angiography and diagnosed blood stasis syndrome of coronary heart disease are given conventional Western medicine treatment and Xuesaitong soft capsule.

干预措施: Xuesaitong soft capsule (Drug)

Placebo Comparator

Placebo Comparator

Patients who confirmed by coronary angiography and diagnosed blood stasis syndrome of coronary heart disease are given conventional Western medicine treatment and placebo.

干预措施: Placebo oral capsule (Drug)

结局指标

主要结局

major adverse cardiovascular events

时间窗: 60 days

death, myocardial infarction, hospitalization for unstable angina or stroke

blood stasis syndrome scale of Coronary heart disease angina pectoris

时间窗: 60

to evaluate patients by blood stasis syndrome scale of Coronary heart disease angina pectoris

Seattle Angina Questionnaire

时间窗: 60 days

to evaluate patients by Seattle Angina Questionnaire

次要结局

  • lipid(60)

研究者

发起方
Jie Wang
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jie Wang

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

Guang'anmen Hospital of China Academy of Chinese Medical Sciences

研究点 (1)

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