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临床试验/ITMCTR2200005711
ITMCTR2200005711招募中4 期

Keganliyan oral liquid in the treatment of acute pharyngitis (externally induced wind-heat syndrome) : a randomized, double-blind, placebo-parallel, multicenter clinical study

Guangdong Provincial Hospital 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
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 65(—)
性别
All

入选标准

  • (1) meet the diagnostic criteria of acute pharyngitis of Western Medicine;
  • (2) meet the diagnostic criteria of wind-heat Syndrome caused by exogenous pathogenic factors of Traditional Chinese Medicine;
  • (3) body temperature =38.5 °c;
  • (4) Pain Vas =4 points;
  • (5) course of Disease =48 hours;
  • (6) age between 18 and 65 years;
  • (7) sign voluntary informed consent.

排除标准

  • (1) patients with NCP positive for nucleic acid or suspected positive for imaging;
  • (2) patients with suppurative Tonsillitis, pneumonia, bronchitis, otitis media, Herpangina, viral myocarditis, acute nephritis, rheumatic joints and other diseases;
  • (3) as a result of measles, scarlet fever, influenza and Agranulocytosis, infectious mononucleosis, leukemia and other pharyngeal symptoms or inflammation;
  • (4) white blood cell count (WBC)=10 * 10 ^ 9/l;
  • (5) those who have used other Chinese and Western medicine for this disease or need to take antibiotics for other diseases within 24 hours;
  • (6) patients with severe primary diseases of heart, cerebral vessels and hemopoietic system, in which AST, ALT > 1.5 n (n is the upper limit of normal value) , serum creatinine (CR) > the upper limit of normal value; patients with malignant tumor;
  • (7) patients with neurological and mental disorders who can not cooperate, or unwilling to cooperate;
  • (8) Allergic Constitution or allergic history to more than two drugs or known ingredients of the drug;
  • (9) pregnant and expectant pregnant or lactating women;
  • (10) participated in other clinical trials in the last 3 months;
  • (11) the researchers did not consider it appropriate to participate in this clinical trial.

研究者

发起方
Guangdong Provincial Hospital of traditional Chinese medicine

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