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
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