Novel Coronavirus Pneumonia (COVID-19)
Conditions
Interventions
Experimental group:honeysuckle decoction
Control group:placebo
Sponsors
Nanjing Second Hospital
Eligibility
Sex/Gender
All
Age
No minimum to 100 Years
Inclusion criteria
Inclusion criteria: 1. Age is not limited; 2. Clinical diagnosis is in accordance with the "Notice on issuing a new type of coronavirus pneumonia diagnosis and treatment program (Fifth edition)" on the diagnosis of a new type of coronavirus infection; 3. potable decoction; 4. no honeysuckle allergy; 5. child-bearing age female subjects pregnancy test negative person; 6. child-bearing age female subjects pregnancy test positive person needs targeted communication, the patient's consent can be included; 7. pregnancy or breast-feeding subjects need targeted communication, the patient's consent can be included in the voluntary informed consent signed by the person under the age of 16.
Exclusion criteria
Exclusion criteria: (1) Those who cannot take Chinese traditional medicine decoction; (2) mentally ill subjects who are not easy to control; (3) those who are pregnant or breast-feeding; (4) those who use other Chinese medicines; (5) those who are not considered suitable to participate in this trial by researchers.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| rate of cure; | — |
Secondary
| Measure | Time frame |
|---|---|
| time to temperature normal;breath symptoms and measure;hospitalization days; | — |
Countries
China
Contacts
Public ContactYongxiang Yi
Nanjing Second Hospital
Outcome results
None listed