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Determination of dandelion capsule on patient with Covid-19 virus

Determination of dandelion herbal capsule (Dandelherb) efficacy on symptom of patient with Covid-19 virus: a clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180513039641N2
Enrollment
80
Registered
2020-07-27
Start date
2020-07-26
Completion date
Unknown
Last updated
2020-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid-19 infectious disease. Coronavirus infection :COVID-19, virus identified (a disease diagnosis of COVID-19 confirmed by laboratory testing)

Interventions

Intervention 1: Intervention group: Oral yellow herbal Dandelion Capsule 300 mg with production license by the Managing Director of Nik Daroie Shafasaz Amiran Company and produced in Booali Daro Pharm

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

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

MeasureTime 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

MeasureTime 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

Public ContactReihaneh Tabaraie

Ghoum University of Medical Sciences

rt1356@yahoo.com+98 25 3612 2000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026