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临床试验/ITMCTR1900002681
ITMCTR1900002681尚未招募未知

The efficacy and safety of Ganduqing granule for treating common cold with qi deficiency leading to lingering of evil syndrome: a randomized, double-blind, placebo, parallel-group, multicenter- controlled trial

Hospital of of Chengdu University of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
尚未招募
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 70(—)
性别
All

入选标准

  • (1) Meet the diagnosis of common cold according to Western medicine;
  • (2) Meet the diagnosis of common cold with qi deficiency syndrome according to Traditional Chinese Medicine;
  • (3) Repeated colds every year, more than 4 times;
  • (4) Symptom presenting within 48 hours;
  • (5) Aged between 18 and 70 years;
  • (6) Voluntarily participate and provide signed informed consent.

排除标准

  • (1) Influenza;
  • (2) Patient's body temperature over 39 degree C;
  • (3) White blood cell count > 12.0 x 10^9/L and/or neutrophil percentage > 80%;
  • (4) Patients with other infectious diseases of the respiratory tract, such as acute herpetic pharyngitis, acute viral pharyngitis, acute herpetic laryngitis, acute viral laryngitis, acute tonsillitis, and pneumonia;
  • (5) Liver function levels (alanine aminotransferase (ALT) and aspartate aminotransferase (AST)) 1.5 times higher than the upper limit of normal or abnormal serum creatinine;
  • (6) Allergic or possibility of being allergic to the ingredients in the study drug;
  • (7) Patients with severe cardio-cerebrovascular, lung, kidney or hematopoietic system diseases;
  • (8) Patients who have participated in other drug clinical trials within one month or are participating in other drug clinical trials;
  • (9) Other medicines (including cold, antibiotics, antivirals and similar traditional Chinese medicines) that have been used to treat the disease since symptom presenting within 48 hours;
  • (10) Pregnant and lactating women;
  • (11) Psychiatric patients;
  • (12) Identified by the investigator as inappropriate to participate in this study.

研究者

发起方
Hospital of of Chengdu University of Traditional Chinese Medicine

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