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临床试验/ITMCTR2000003142
ITMCTR2000003142尚未招募未知

Efficacy and safety of Chinese Herb Medicine Hua-Shi Bai-Du granules in patients with novel coronavirus pneumonia (COVID-19) in Wuhan, China: a prospective, randomized, controlled, open-label trial

Guangdong Provincial Hospital 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
未知
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 85(—)
性别
All

入选标准

  • (1) Meet the diagnostic criteria for patients with COVID-19 of the Proposal of Diagnosis and Treatment of COVID-19;
  • (2) Aged 18-85 years;
  • (3) To agree to participate in the study and sign the informed consent

排除标准

  • (1) Critical patients;
  • (2) TCM diagnosis of yang deficiency syndrome, manifested as limb warm, thin stools, chills, etc.;
  • (3) Patients who cannot guarantee compliance during treatment, and patients who are difficult to administer by oral or nasal route;
  • (4) Patients with severe primary respiratory disease or other pathogenic microbial pneumonia that needs to be identified with COVID-19;
  • (5) Pregnant and mothers, those who have a pregnancy plan, and those who have a positive urine pregnancy test;
  • (6) Patients with other systemic malignant diseases such as malignant tumors, mental illnesses, etc., which the researchers consider unsuitable for participation in the study;
  • (7) People who have been allergic to Chinese medicine or intolerant to taking medicine.
  • (8) Patients are participating in other COVID-19 clinical trials.

研究者

发起方
Guangdong Provincial Hospital of Chinese Medicine

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