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临床试验/NCT03792035
NCT03792035Unknown4 期

China Tongxinluo Study for Myocardial Protection in Patients With Acute Myocardial Infarction

China National Center for Cardiovascular Diseases7 个研究点 分布在 1 个国家目标入组 3,796 人开始时间: 2019年5月23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
3,796
试验地点
7
主要终点
MACCE

研究概览

简要总结

To determine the therapeutic effects of Tongxinluo Capsules as compared with placebo in the treatment of patients with acute ST-elevation myocardial infarction (STEMI): (1) Clinical efficacy and safety at 30 days: the incidence of composite endpoints comprising major adverse cardiovascular and cerebrovascular events (MACCE, including cardiovascular death, myocardial re-infarction, emergency coronary revascularization and cerebral stroke), severe complications (including cardiogenic shock, heart failure, mechanical complications and malignant arrhythmias), and major bleeding (BARC grade III and V); (2) Clinical efficacy and safety at 1 year: the incidence of composite endpoints comprising MACCE, hospitalization due to heart failure, in-stent thrombosis, and major bleeding (BARC grade III and V), as well as all-cause mortality; (3) the effects in promoting myocardial reperfusion, reducing incidence of myocardial no-reflow, protecting ischemic myocardium, minimizing infarction size, and improving left ventricular systolic function.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age>18 years;
  • Within 24 hours of infarctional chest pain onset;
  • ECG shows ST-segment elevation ≥0.2mV in more than 2 adjacent leads, or new left bundle branch block (LBBB);
  • Voluntary participation in the study with consent forms signed.

排除标准

  • Critically illness due to STEMI;
  • Long-term (>20 min) cardio-pulmonary resuscitation (CPR);
  • Suspected aortic dissection or acute pulmonary embolism;
  • Explicit mechanical complications, including interventricular septum perforation, rupture of papillary muscles and chordae tendineae, or on-going or ruptured left ventricular free walls.
  • Serious cardiogenic shock and do not responding to hypertensive agents;
  • Uncontrolled acute left heart failure or pulmonary edema;
  • Malignant arrhythmias uncontrolled by anti-arrhythmia agents;
  • Bleeding history of cerebral vessels, gastrointestinal tract, respiratory tract, urinary tract or other organs within 1 month;
  • Presence of active hemorrhage at any part of the body (including menstruation);
  • Known hemorrhagic constitution or serious hemostasis and blood coagulation disorders;
  • Current usage of anticoagulants (such as Warfarin or new anticoagulants);
  • . Serious hepatorenal dysfunction [ATL≥5 ULN (upper limit of normal), Cr>134μmol/L (2mg%) or eGFR<45ml/min/1.73m2];
  • Serious chronic obstructive pulmonary disease (COPD) or respiratory failure;
  • . Severe infection:
  • . Very weak or frailty;
  • . Neuropsychiatric system diseases;
  • . Malignancies;
  • . Other pathophysiological conditions with expected survival time <1 year;
  • Allergy to the ingredients of this investigational drug;
  • Women who are in pregnancy or nursery;
  • Participation in clinical study of other traditional Chinese medicine (TCM);
  • Unsuitability to participate in this study due to other diseases.

研究组 & 干预措施

Experimental group

Experimental

First time given 8 capsules of Tongxinluo, then given 4 capsules of Tongxinluo, tid, po.Dosage form: capsule;Dose: 0.26g/capsule;Duration:1 year

干预措施: Tongxinluo (Drug)

Control group

Placebo Comparator

First time given 8 capsules of placebo, then given 4 capsules of placebo, tid, po.Dosage form: capsule;Dose: 0.26g/capsule;Duration:1 year

干预措施: Placebos (Drug)

结局指标

主要结局

MACCE

时间窗: 30-day

30-day incidence of composite endpoint events comprising MACCE (including cardiovascular death, myocardial re-infarction, emergency coronary revascularization and cerebral stroke)

次要结局

  • Revascularization(30-day)
  • Cerebral stroke(30-day)
  • STEMI(30-day)
  • The incidence of bleeding in BARC(Bleeding Academic Research Committee Bleeding Standard) III and V(30-day)
  • MACCE(1 year)
  • In-stent restenosis(1 year)
  • All-cause mortality rate at 1 year(1 year)
  • Myocardial reperfusion and no-reflow(2 hours, 24 hours and 7 days)

研究者

发起方
China National Center for Cardiovascular Diseases
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

fuwaihospital

Assistant dean

China National Center for Cardiovascular Diseases

研究点 (7)

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