A randomized controlled prospective study of Reyanning mixture in the treatment of mild novel coronavirus pneumonia (COVID-19)
- Conditions
- ovel Coronavirus Pneumonia (COVID-19)
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- Not specified
In accordance with the Novel Coronavirus Diagnosis and Treatment Protocol (Trial Version 9) issued by the National Health Commission Diagnosis of mild COVID-19; Signed informed consent.
1. Patients with normal, severe or critical type of NCOV infection; 2. Other lung diseases; 3. Patients with serious primary diseases such as heart, brain, liver, kidney and hematopoietic system; 4. Patients with basic lung diseases such as severe interstitial lung lesions confirmed by chest CT; 5. People who cannot cooperate in mental state, suffer from mental diseases, cannot control themselves and cannot express themselves clearly; 6. Allergic constitution (such as allergic to two or more drugs or food) or allergic history of this product and conventional treatment drugs; 7. Pregnant or lactating women.
Study & Design
- Study Type
- Interventional study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ucleic acid turning negative time;Nucleic acid conversion rate;
- Secondary Outcome Measures
Name Time Method TCM syndrome scoring Scale;Factors of TCM diagnosis syndrome;Tongue and pulse survey of TCM;