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

Phase 3

Recruiting

• Conditions: Diuretic effect.; Other diuretics; Y54.5

• Registration Number: IRCT20180513039641N3
• Lead Sponsor: Ghoum University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 1 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

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

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)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
rine 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.