Clinical Trial Details

Trial ID: L0457
Source ID: IRCT20180802040678N2
Associated Drug: Piperine
Title: Investigation of the effect of piperine supplement on anthropometric indices, ultrasonographic findings, biochemical parameters and quality of life in patients with nonalcoholic fatty liver disease
Acronym: --
Status: Recruiting
Study Results: No Results Available
Results: --
Conditions: Non-Alcoholic Fatty Liver Disease. <br>Fatty (change of) liver, not elsewhere classified;K76.0
Interventions: Intervention 1: Intervention group: Administration of Piperine 5mg supplement daily for three months. Intervention 2: Control group: Administration of placebo for three months.
Outcome Measures: Fattly Liver Grading. Timepoint: Before and after intervention. Method of measurement: Ultrasonography.;Quality of Life. Timepoint: Before and after intervention. Method of measurement: SF-36, CLDQ, and Disease Symptom Index 2.0 questionnaires.;Anthropometric indices. Timepoint: Before and after intervention. Method of measurement: Body weight and Body Mass Index.;Biochemical parameters. Timepoint: Before and after intervention. Method of measurement: Aspartate Aminotransferase, Alanine Aminotransferase, Alkaline Phosphatase, Bilirubin Total and Direct, Fasting Blood Suger, Triglyceride, LDL, HDL, VLDL, Hs-CRP, Total Cholesterol, Albumin, Count Blood Cells, HbA1C, HOMA-IR, Fecal Calprotectin.nan
Sponsor/Collaborators: Tabriz University of Medical Sciences
Gender: All
Age: 18 yearsno limit
Phases: Phase 3
Enrollment: 64
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Randomization description: Block randomizing by computer software, Blinding description: Participants-healthcare provider-data collectors.
Start Date: 13/08/2019
Completion Date: --
Results First Posted: --
Last Update Posted: 7 October 2019
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/41203