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Studying of the diuretic effect of Dandelion herbal capsule (Dandelherb)

Studying of the diuretic effect of Dandelion herbal capsule (Dandelherb) in healthy people during one day: A clinical trial study

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180513039641N3
Enrollment
60
Registered
2023-04-11
Start date
2023-04-21
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Diuretic effect. Other diuretics

Interventions

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

Sponsors

Ghoum University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Healthy people in the age range of 18-65 years (by referring to the health center) who have a GFR above 60% by creatinine test.

Exclusion criteria

Exclusion criteria: History of allergy to plants of asteraceae. People with bile duct or intestinal obstruction People with acute cholecystitis, empyema, acute gall bladder inflammation People who have digestive diseases, gastritis, irritable bowel syndrome People with diabetes and kidney failure Pregnant and lactating women and Married women who are in childbearing age and do not use reliable contraception method Weight below 50 kg Patients with uncontrolled underlying diseases such as hypertension and... Patients who take medications that interfere with dandelion herbal capsules. Medicines such as: 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 omeprazole People who take the following herbs: bloodroot, cat's paw, chamomile, chaparral, fennel, samiana, Echinacea angustifolia, gorse, grapefruit juice, licorice, oregano, red clover, St. John's wort, wild cherry, and yucca. Alcohol consumption history (more than 10 grams per day for women and more than 20 grams per day for men)

Design outcomes

Primary

MeasureTime frame
Urine volume. Timepoint: The first day of the study (negative 2), the second day of the study (negative 1), the third day of the study (intervention day=day zero), the fourth day (tomorrow of the intervention day=day 1). Method of measurement: Collect in the included containers.;Urinary frequency. Timepoint: The first day of the study (negative 2), the second day of the study (negative 1), the third day of the study (intervention day=day zero), the fourth day (tomorrow of the intervention day=day 1). Method of measurement: counting.;Amount of fluids consumed. Timepoint: The first day of the study (negative 2), the second day of the study (negative 1), the third day of the study (intervention day=day zero), the fourth day (tomorrow of the intervention day=day 1). Method of measurement: Record.

Countries

Iran (Islamic Republic of)

Contacts

Public Contacthoda Abolhasani

Ghoum University of Medical Sciences

hodaabolhasani@gmail.com+98 25 3320 9071

Outcome results

None listed

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