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临床试验/ITMCTR2000003080
ITMCTR2000003080尚未招募1 期

Study for the Effectiveness and Safety of Yi-Qi Hua-shi Jie-Du-Fang in the Treatment of the Novel Coronavirus Pneumonia (COVID-19)

Affiliated Hospital of traditional Chinese and Western Medicine Nanjing University of 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
18 至 75(—)
性别
All

入选标准

  • 1) Confirmed or clinically diagnosed patients with the novel coronavirus disease;
  • 2) Those who have been identified by Chinese medicine as pestilence stagnant in Lung;
  • 3) Inpatients aged 18 to 75 years male or female;
  • 4) Volunteer to receive treatment under their own scheme and sign informed consent.

排除标准

  • 1) Patients with mild, severe or critical novel coronavirus disease;
  • 2) According to the researcher's judgment, previous or current diseases may affect patients' participation in the trial or influence the outcome of the study, including: malignant disease, autoimmune disease, severe malnutrition, liver and kidney disease, blood disease, nervous system Diseases and endocrine diseases; currently suffering from diseases that seriously affect the immune system, such as: human immunodeficiency virus (HIV) infection, or the blood system, or splenectomy, organ transplantation, etc .;
  • 3) Those who are allergic to the research drug and its main ingredients;
  • 4) pregnant or lactating women;
  • 5) Those who have difficulty taking medicine orally.

研究者

发起方
Affiliated Hospital of traditional Chinese and Western Medicine Nanjing University of Chinese Medicine

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