Clinical Trial Details

Trial ID: L0779
Source ID: IRCT20180404039187N2
Associated Drug: Allopurinol
Title: study the effects of Allopurinol on liver enzymes and grade of fatty liver on ultrasound in patients with non-alcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: non-alcoholic fatty liver disease. <br>Fatty (change of) liver, not elsewhere classified
Interventions: Intervention 1: Intervention group: consumption of 100 mg Allopurinol daily for 6 months. Intervention 2: Control group: routin care.
Outcome Measures: Serum liver enzymes AST and ALT and grade of fatty liver based on ultrasound. Timepoint: at the beginning and 3 and 6 months later. Method of measurement: laboratory tests and ultrasound.nan
Sponsor/Collaborators: Tabriz University of Medical Sciences
Gender: All
Age: 18 years65 years
Phases: Phase 3
Enrollment: 100
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Randomization description: Arrange the accident stages: 1) Determine the volume of each block (Foursquare blocks) 2) Prepare block lists and
Start Date: 23/11/2018
Completion Date: --
Results First Posted: --
Last Update Posted: 14 January 2019
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/32805