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临床试验/ITMCTR2100004678
ITMCTR2100004678招募中4 期

A randomized double-blind controlled clinical study on the effects of qishen yiqi dropping pills on exercise endurance and quality of life in patients with coronary heart disease after interventional therapy

China-Japan Friendship Hospital0 个研究点开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
招募中
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional study

入排标准

年龄范围
18 至 75(—)
性别
All

入选标准

  • 1. Have a clear understanding of the research content and purpose, participate in the study voluntarily, and sign the informed consent form by himself / herself;
  • 2. It is consistent with the diagnostic criteria of Western medicine for stable coronary heart disease;
  • 3. Patients with Qi deficiency and blood stasis syndrome who meet the above diagnostic criteria of TCM;
  • 4. Complete the overall treatment plan after PCI;
  • 5. Within 1 week to 6 months after PCI;
  • 6. The age is between 18 and 75 years old.

排除标准

  • 1. There are contraindications of cardiopulmonary exercise test;
  • 2. Plan for coronary artery bypass grafting or heart transplantation;
  • 3. Within 3 months before admission: stroke, transient ischemic attack; carotid artery or other major vascular surgery; persistent ventricular tachycardia or ventricular fibrillation;
  • 4. Ventricular arrhythmia was not controlled effectively (antiarrhythmic drugs or implantable defibrillator were ineffective;
  • 5. Uncorrected primary obstruction or severe reflux valvular disease, non dilated (restrictive) or hypertrophic cardiomyopathy;
  • 6. Patients with second or third degree heart block or sick sinus syndrome, without permanent pacemaker, who need implantable devices for heart failure;
  • 7. Obstructive or bronchospasmodic lung disease (such as asthma, bronchitis, etc.) requires oral or inhaled bronchodilator or hormone therapy;
  • 8. Pregnant or lactating women and women who plan to become pregnant during the trial period;
  • 9. Cancer or other systemic diseases, the expected survival time is less than 12 months;
  • 10. Use other clinical trial drugs or participate in medical device test within 30 days before enrollment;
  • 11. The researchers considered that they could not participate in the study after clinical evaluation.

研究者

发起方
China-Japan Friendship Hospital

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