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临床试验/ITMCTR2100004863
ITMCTR2100004863招募中1 期

Research on key generic technologies and application of community prevention and control of chronic diseases related to phlegm and blood stasis

Institute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
1 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
40 至 80(—)
性别
All

入选标准

  • 1. Aged 40-80 years, male or female;
  • 2. The diagnostic criteria for unstable angina pectoris were confirmed by the researchers in the Guidelines for Rapid Emergency Diagnosis and Treatment of Acute Coronary Syndrome (2019) published by the Chinese Medical Doctor Association Emergency Physicians Branch in 2019.
  • 3. Global Registry of Acute Coronary Events (GRACE) risk score 2.0(18) in-hospital models; the patients will be judged as low-risk or medium-risk or high-risk patients (GRACE score < 140) by the researchers.
  • 4. According to the main symptoms in the Diagnosing Items of Heat Retention Blood Vessel Syndrome of Coronary Heart Disease developed by our research group, the patients were judged by the researchers to be the patients with hot crunch;
  • 5. Signed the informed consent and volunteered to participate in the study.

排除标准

  • 1. Patients with congenital organic heart disease, severe myocardial disease and severe cardiopulmonary dysfunction;
  • 2. Severe arrhythmias (rapid atrial fibrillation, atrial flutter, paroxysmal ventricular tachycardia, etc.) with hemodynamic changes;
  • 3. Complicated with severe liver (ALT or AST > 1.5 times the upper limit of normal value), kidney (CR BBB>per limit of normal value) dysfunction or severe blood disease, or other serious diseases affecting survival;
  • 4. Patients with poor hypertension control (systolic blood pressure >= 160mm Hg, and/or diastolic blood pressure >= 100mm Hg);
  • 5. Patients with high blood risk, including patients with congenital bleeding diseases (such as hemophilia), thrombocytopenia (platelet count less than 30 x 10^9/L) or patients with platelet dysfunction, or patients with coagulation disorders whose PT/APTT is higher than the upper limit of normal value);
  • 6. Patients with severe cognitive impairment or mental disorder, unable to complete the subject's knowledge, unable to cooperate with clinical treatment and evaluation;
  • 7. Pregnant or lactating women, or patients who intend to have children during the study period;
  • 8. Participated in or is participating in other clinical trials within the last three months;
  • 9. Patients who need to take Gansui, Jingdaji, Haizao, Yuanhua and Lilu during medication period;
  • 10. Patients unsuitable for inclusion or unsuitable for other reasons as determined by the researcher.

研究者

发起方
Institute of Basic Theory for Chinese Medicine, China Academy of Chinese Medical Sciences

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