ITMCTR2200006404尚未招募1 期
Randomized multi-center clinical efficacy evaluation of Chinese medicine intervention on children respiratory syncytial virus pneumonia
The Affiliated Hospital of Liaoning 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
- 1 期
- 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
- 1 至 5(—)
- 性别
- All
入选标准
- •1.Children who meet the diagnosis of respiratory syncytial virus pneumonia;
- •2.Children who meet the TCM diagnosed pneumonia with dyspneic cough with syndrome of heat pathogen blocking lung;
- •3.Aged from 1 to 5;
- •4.The course of RSV pneumonia is within 48 hours;
- •5.The legal guardian and the child who can understand and sign his/her name have understood and signed the informed consent.
排除标准
- •1. Drugs taken within 24 hours before onset that may affect the efficacy evaluation of the test (such as antipyretic and analgesic drugs, antibacterial drugs, H1 receptor blockers, vasoconstrictor and Traditional Chinese medicines with the same efficacy as the test drugs, etc.);
- •2. Severe pneumonia in children (according to the criteria for classification of severity according to 2013 Guidelines for The Management of Community-acquired Pneumonia in Children);
- •3. Patients with onset of other respiratory diseases except pneumonia;
- •4. Allergic to the test drug;
- •5. Patients who have participated in or are participating in clinical trials of other drugs within the last 3 months;
- •6. According to the doctor's judgment, it is easy to lose visitors.
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