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

Phase 1
Not yet recruiting
Conditions
ovel Coronavirus Pneumonia (COVID-19)
Registration Number
ITMCTR2000003080
Lead Sponsor
Affiliated Hospital of traditional Chinese and Western Medicine Nanjing University of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

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.

Exclusion Criteria

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.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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