ITMCTR2000003243尚未招募1 期
Study for efficacy and safety of Jie-Xing-Jun-Zi granules in the Treatment of convalescent patients of novel coronavious pneumonia (COVID-19)
Beijing University of Chinese Medicine Third Affiliated Hospital0 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
- 18 至 75（—）
- 性别
- All
入选标准
- •(1) Convalescent patients with novel coronavious pneumonia,and the patient is aged 18-75 years old;
- •(2) The TCM syndrome type conforms to deficiency of 'qi' and 'yin' and not exhausted of 'Yu Xie';
- •(3) Voluntary test, or the immediate family or the client's approved client agrees to the test, and voluntarily signs the informed consent;
- •(4) Provide detailed contact information, no short-term willingness to move and be willing to cooperate with followers.
排除标准
- •(1) Patients with fasting water due to gastrointestinal bleeding, intestinal obstruction, etc;
- •(2) Patients with pre-existing severe brain, heart, liver, kidney and hematopoietic system diseases;
- •(3) Patients who are known to be allergic to the ingredients of the intervention drug;
- •(4) Patients who are unable to cooperate with follow-up.
研究者
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