Clinical Trial Details

Trial ID: L0462
Source ID: IRCT20190714044196N1
Associated Drug: Berberis
Title: The effect of hydroalcoholic extract of Berberis fruits integerrima on the lipid profile, antioxidantparameters and liver and kidney function tests in patients with nonalcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic fatty liver. <br>Fatty (change of) liver, not elsewhere classified;K76.0
Interventions: Intervention 1: Intervention group: received a gelatin capsule contain 750 mg hydro-alcoholic extract of Berberis integerrima . Berberis fruits were taken from mountainous areas of Bardsir, Kerman, Southeast of Iran and confirmed by Iranian institute of r
Outcome Measures: Fasting blood glucose. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Total cholesterol. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Triglyceride. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;LDL-C. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;HDL-C. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Alanine aminotransferase. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Aspartate aminotransferase. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Alkaline phosphatase. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Total bilirubin. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;And direct bilirubin. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Urea. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Creatinine. Timepoint: Before and after treatment. Method of measurement: measured using Pars azmun kit.;Glutathione peroxidase enzyme. Timepoint: Before and after treatment. Method of measurement: ZellBio kit.;Malondialdehyde. Timepoint: Before and after treatment. Method of measurement: ZellBio kit.;Total antioxidant. Timepoint: Before and after treatment. Method of measurement: ZellBio kit.;Blood pressure. Timepoint: Before and after treatment. Method of measurement: Blood pressure monitor.nan
Sponsor/Collaborators: Rafsanjan University of Medical Sciences
Gender: All
Age: 20 years45 years
Phases: Phase 3
Enrollment: 42
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Randomization description: Patients separated to two groups, randomly using table of random numbers, Blinding description: Participant (patients
Start Date: 31/07/2019
Completion Date: --
Results First Posted: --
Last Update Posted: 7 October 2019
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/40780