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
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