Clinical Trial Details

Trial ID: L0726
Source ID: IRCT20120415009472N19
Associated Drug: Rosemary
Title: Effects of Rosemary (Rosmarinus officinalis) Leaves Powder And Weight Reducing Diet on Hs-CRP, MDA, TAC, Blood Pressure, Anthropometric measurement, Quality of life, Sleep and Appetite in Patients with Non-Alcoholic Fatty Liver Disease
Acronym: --
Status: Recruiting
Study Results: No Results Available
Results: --
Conditions: Nonalcoholic fatty liver disease. <br>Fatty (change of) liver, not elsewhere classified;K76.0
Interventions: Intervention 1: Intervention group (n = 60): Low-calorie diet and physical activity design based on the Adult Overweight and Obesity Control Guide (published by the US National Heart, Lung, and Blood Institute). The low-calorie diet will be calculated as
Outcome Measures: Malondialdehyde. Timepoint: Before intervention and 8 weak after intervention. Method of measurement: Colorimetric method.;Total Antioxidant Capacity. Timepoint: Before intervention and 8 weak after intervention. Method of measurement: Colorimetric method.;High sensitivity C-reactive protein. Timepoint: Before intervention and 12 weak after intervention. Method of measurement: Turbidometric method.Systolic blood pressure. Timepoint: Before intervention and 8 weak after intervention. Method of measurement: Mercury barometric.;Diastolic blood pressure. Timepoint: Before intervention and 8 months after intervention. Method of measurement: Mercury barometric.;Weight. Timepoint: Before intervention and 8 months after intervention. Method of measurement: Scales.;Waist. Timepoint: Before intervention and 8 months after intervention. Method of measurement: Meter.;Hip circumference. Timepoint: Before intervention and 8 months after intervention. Method of measurement: Meter.;Waist to hip ratio. Timepoint: Before intervention and 8 months after intervention. Method of measurement: calculation.;Body fat percentage. Timepoint: Before intervention and 8 months after intervention. Method of measurement: inbody.;BMI. Timepoint: Before intervention and 8 months after intervention. Method of measurement: calculation.;Quality of Life. Timepoint: Before intervention and 8 months after intervention. Method of measurement: SF-36 questionnaire.;Sleep quality. Timepoint: Before intervention and 8 months after intervention. Method of measurement: The Pittsburgh Sleep Quality questionnaire.;Appetite. Timepoint: Before intervention and 8 months after intervention. Method of measurement: CNAQ questionnaire.
Sponsor/Collaborators: Vice-chancellor for research Iran University of Medical Sciences
Gender: All
Age: 20 years65 years
Phases: Phase 2
Enrollment: 120
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Supportive, Randomization description: In this research, patients referred to the Gastroenterology and Liver Clinic of Razi Hospital in Rasht will be select
Start Date: 14/10/2019
Completion Date: --
Results First Posted: --
Last Update Posted: 5 November 2019
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/36981