Official Title
Traditional Chinese Medicine or Low-dose Dexamethasone in Symptomatic Patients With Post-COVID-19 Parenchymal Lung Abnormalities: a Randomized Controlled Trial Three Arm, Parallel Group, Single Blind, Randomized Controlled Trial.
Brief Summary

The goal of this type of clinical trial is to learn about symptomatic patients withpost-COVID-19 parenchymal lung abnormalities. The main questions it aims to answer are:the efficacy and safety of low-dose dexamethasone or traditional Chinese medicine insymptomatic patients with post-COVID-19 parenchymal lung abnormalities.Participants will be divided into three parallel groups:controlled group withconventional western medicine treatment including oxygen therapy, antibiotics,nebulization therapy, etc. dexamethasone group: dexamethasone 1.5mg/day for one week and0.75mg/day for another week basing on conventional western medicine. Chinese medicinegroup: Strengthening spleen and tonifying lung decoction for 2 weeks basing onconventional western medicine.

Detailed Description

Not Provided

Recruiting
COVID-19 Pneumonia

Other: conventional western medicine treatment

conventional western medicine treatment only

Drug: Dexamethasone oral tablet

treat with Dexamethasone for 2 weeks

Other: Traditional Chinese medicine decoction

treat with strengthening spleen and tonifying lung decoction for 2 weeks

Eligibility Criteria

Inclusion Criteria:

- Clinical diagnosis of COVID-19 pneumonia;

- 3 to 8 weeks after the onset of the first symptoms of COVID-19 infection;

- Modified Medical Research Council (mMRC) score ⩾2 or hypoxemia;

- Imaging severity assessment of pneumonia: CT severity scores (CTSS):≥5;

- Signed the informed consent.

Exclusion Criteria:

- Participants still admitted to intensive care unit at the time of enrollment;

- Known prior structural lung disease, including pulmonary fibrosis, severe COPD,
severe bronchiectasis, and lung destruction;

- Taking glucocorticoids or immunosuppressants because of other chronic diseases;

- Contraindications of glucocorticoid;

- Heart failure(NYHA III or IV);

- Participants with renal replacement therapy;

- Psychiatric disorders or cognitive impairments;

- The expected survival time is less than six months due to diseases other than
COVID-19 pneumonia.

Eligibility Gender
All
Eligibility Age
Minimum: 18 Years ~ Maximum: N/A
Countries
China
Locations

China-Japan Friendship Hospital
Beijing, Beijing, China

Investigator: Wanmu Xie, Doctor
Contact: 86-10-84206246
xiewanmu@126.com

Contacts

Wanmu Xie, Doctor
86-10-84206246
xiewanmu@126.com

Zhenguo Zhai, Dcotor, Principal Investigator
Department of Respiratory and Critical Care Medicine

China-Japan Friendship Hospital
NCT Number
MeSH Terms
COVID-19
Pneumonia
Dexamethasone