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临床试验/ITMCTR1900002675
ITMCTR1900002675招募中4 期

Randomized controlled clinical trial for the efficacy and safety of Kaihoujian inhalation for acute laryngitis

Wangjing Hospital, 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
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) Patients meets the standard of Western medicine acute laryngitis (light and moderate);
  • (2) Patients meets the standard of Chinese medicine of wind-heat invading lung;
  • (3) Aged 18 to 65 years;
  • (4) Patients who first visit ENT clinicians within 48 hours;
  • (5) Patients who signed the informed consent form.

排除标准

  • (1) Those with a body temperature higher than 37 degree C;
  • (2) Those with common cold, influenza, acute tonsillitis, pharyngeal diphtheria, and Wensang's angina;
  • (3) Those with acute tracheal-bronchitis, pneumonia, rheumatic fever , acute glomerulonephritis, rheumatic heart disease and other diseases;
  • (4) Patients with severe primary diseases such as cardiovascular and endocrine or hematopoietic system and those with mental illness;
  • (5) Patients with abnormal liver and kidney function tests, diabetes
  • (6) WBC >= 1.2×10^9/L;
  • (7) Pregnancy (defined as positive for pregnancy test), lactating woman or birth plan within half a year;
  • (8) Accepted Chinese medicines or antibiotics who has similar efficacy in test drugs within 48 hours before enrollment;
  • (9) Those who are participating in other drug clinical trials or known to be allergic to therapeutic drugs;
  • (10) Those who believe that they are not suitable for the test;
  • (11) Patients with obvious laryngeal mucosal edema by electronic laryngoscope.

研究者

发起方
Wangjing Hospital, China Academy of Chinese Medical Sciences

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