Covid-19 infectious disease. Coronavirus infection :COVID-19, virus identified (a disease diagnosis of COVID-19 confirmed by laboratory testing)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients Hospitalized in shaheed Beheshti Hospital in Qom with Covid-19 (their PCR test is positive). Patients between 18-65 years. Satisfaction of people to test this drug and its possible side effects.
Exclusion criteria
Exclusion criteria: History of allergy to plants of asteraceae. bile duct and intestinal obstruction. acute cholecystitis, empyema, acute gall bladder inflammation. Gastrointestinal diseases, gastritis, irritable bowel syndrome. Diabetes and kidney failure. Alcohol consumption history (more than 10 grams per day for women and more than 20 grams per day for men). Pregnant and lactating women and Married women who are in childbearing age and do not use reliable contraception method. Weight below 50 kg Uncontrolled underlying diseases such as high blood pressure and .... Consumers of Lithium, digoxin, corticosteroids such as prednisone, niacin / nicotinic acid, metronidazole, disulfiram, tetracycline and fluoroquinolone antibiotics (such as ciprofloxacin), hypoglycemic drugs, antiplatelet drugs, diuretics, Antacids such as famotidine and s omeprazole. Consumers of s bloodroot, cat’s claw, chamomile, chaparral, chasteberry, damiana, Echinacea angustifolia, goldenseal, grapefruit juice, licorice, oregano, redclover,St.John’swort, wildcherry, andyucca.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| C-Reactive Protein. Timepoint: Measurement of C-Reactive Protein at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood test.;White blood cell. Timepoint: Measurement of white blood cell at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood test.;Red blood cell. Timepoint: Measurement of Red blood cell at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood Test.;Hemoglobin. Timepoint: Measurement of hemoglobin at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood test.;Albumin. Timepoint: Measurement of Albumin at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood Test.;Alanine aminotransferase. Timepoint: Measurement of Alanine aminotransferase at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood Test.;Aspartate transaminase. Timepoint: Measurement of Aspartate transaminase at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood Test.;Creatinine. Timepoint: Measurement of Creatinine at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood Test.;Blood Urea Nitrogen. Timepoint: Measurement of Blood Urea Nitrogen at the beginning of the study (before the start of the study) and 40 days after the start of dandelion capsule. Method of measurement: Blood Test.;Total Bilirubin. Timepoint: Measurement of Total Bilirubin at the beginning of the study (before the start of the study) and 40 days aft | — |
Secondary
| Measure | Time frame |
|---|---|
| High sensitivity C-Reactive Protein. Timepoint: Before and after medication with Dandelion cap. Method of measurement: Blood Test. | — |
Countries
Iran (Islamic Republic of)
Contacts
Ghoum University of Medical Sciences