Official Title
The Efficacy and Safety of Huai er in the Adjuvant Treatment of COVID-19: a Prospective, Multicenter, Randomized, Parallel Controlled Clinical Study
Brief Summary

In December 2019,a new type of pneumonia caused by the coronavirus (COVID-2019) broke out in Wuhan ,China, and spreads quickly to other Chinese cities and 28 countries. More than 70000 people were infected and over 2000 people died all over the world.There is no specific drug treatment for this disease. This study is planned to observe the efficacy and safety of Huaier granule in the adjuvant treatment COVID-19.

Unknown status
COVID-19

Drug: Huaier Granule

standard treatment + Huaier Granule 20g po tid for 2weeks

Eligibility Criteria

Inclusion Criteria:

1. Aged between 18 and 75 years, extremes included, male or female

2. Patients diagnosed with mild or common type COVID-19, according to the official
guideline "Pneumonia Diagnosis and Treatment Scheme for Novel Coronavirus Infection
(Trial Version 6)"

3. patients can generally tolerable for treatment recommended by the official guideline
"Pneumonia Diagnosis and Treatment Scheme for Novel Coronavirus Infection (Trial
Version 6)"

4. Patients have not been accompanied by serious physical diseases of heart, lung, brain,
etc.,Eastern Cooperative Oncology Group score standard:0-1

5. Ability to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

1. Female subjects who are pregnant or breastfeeding.

2. patients who are allergic to this medicine

3. patients meet the contraindications of Huaier granule

4. Patients with diabetes

5. Patients have any condition that in the judgement of the Investigators would make the
subject inappropriate for entry into this study.

6. patients can't take drugs orally

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: 75 Years
Contacts

Lin Chen
+8613517260864
chenlin_tj@126.com

Tongji Hospital
NCT Number
Keywords
Covid-19
Huaier granule
MeSH Terms
COVID-19