Coronavirus disease. COVID-19, virus identified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients with COVID-19 Twice positive PCR test Age over 20 years Provide written consent to enter the study Not participating in other clinical trials no use of other types of herbal teas
Exclusion criteria
Exclusion criteria: Pregnancy or breastfeeding Obesity(body mass index more than30 kg per square meter ) History of heart attack or stroke, history of coronary bypass graft or coronary angioplasty, hospitalization history with heart failure Underlying diseases including chronic hepatitis, cirrhosis and cholestatic liver disease and severe renal failure Chronic obstructive pulmonary disease or severe pneumonia Active gastrointestinal ulcers
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Severity of the viral infection clinical symptoms. Timepoint: At the beginning of the study and 7, 14 and 21 days after tea consumption. Method of measurement: The severity of clinical signs of viral infection will be detected through a respiratory rate more than 24 or a heart rate greater than 125 or the patient requires mechanical ventilation or saturation of peripheral oxygen less than 94% and also based on the patient's laboratory results including D- dimer more than 1000; creatinine phosphokinase twice the normal amount; positive troponin; progressive lymphopenia; ferritin more than 300.;Complete blood cell count and diffrential count. Timepoint: At the beginning of the study and one month later. Method of measurement: Cell counter devices.;C-reactive protein. Timepoint: At the beginning of the study and one month later. Method of measurement: ELISA device.;Lactate dehydrogenase. Timepoint: At the beginning of the study and one month later. Method of measurement: Biochemical autoanalyzer.;Creatinine phosphokinase. Timepoint: At the beginning of the study and one month later. Method of measurement: Biochemical autoanalyzer.;Troponin. Timepoint: At the beginning of the study and one month later. Method of measurement: ELISA device.;D-dimer. Timepoint: At the beginning of the study and one month later. Method of measurement: ELISA device.;Ferritin. Timepoint: At the beginning of the study and one month later. Method of measurement: ELISA device. | — |
Secondary
| Measure | Time frame |
|---|---|
| Depression score based on Patients Health Questionnaire-9. Timepoint: At the beginning of the study and one month later. Method of measurement: Patients Health Questionnaire-9.;Scale of fatigue based on Chalder Fatigue Scale (CFQ-11). Timepoint: At the beginning of the study and one month later. Method of measurement: Chalder Fatigue Scale (CFQ-11) Questionnaire.;Scale of anxiety based on State-Trait Anxiety Inventory (STAI) Questionnaire. Timepoint: At the beginning of the study and one month later. Method of measurement: State-Trait Anxiety Inventory (STAI) Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Rasht University of Medical Sciences