Clinical Trial Details

Trial ID: L0450
Source ID: IRCT20191006044994N1
Associated Drug: Rosa damascena
Title: Comparison of the effect of Rosa damascena with placebo on liver enzymes in patients with nonalcoholic fatty liver disease(NAFLD): a double-blind randomized clinical trial
Acronym: --
Status: Recruiting
Study Results: No Results Available
Results: --
Conditions: Non Alcoholic Fatty Liver Disease. <br>Non Alcoholic Fatty Liver Disease;k76.0
Interventions: Intervention 1: Intervention group: 500 mg capsules of Rosa damascena,6 capsules per day ;each time 2 capsules(*3), Orally, For12 weeks. Intervention 2: Control group: Placebo (breadcrumbs), 500 mg capsule containing breadcrumbs, 6 capsules daily, three
Outcome Measures: Alt(Alanin transaminase). Timepoint: Onset and 12th week of study(End of study). Method of measurement: Hitachi-912 biochemistery instrument.;Ast(Aspartate transaminase). Timepoint: Onset and 12th week of study(End of study). Method of measurement: Hitachi-912 biochemistery instrument.nan
Sponsor/Collaborators: Iran University of Medical Sciences
Gender: All
Age: 18 years80 years
Phases: Phase 2/Phase 3
Enrollment: 80
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment, Randomization description: The block randomization method is used using 4-way blocks and a random number table.Interventions A and B define six b
Start Date: 11/11/2019
Completion Date: --
Results First Posted: --
Last Update Posted: 17 December 2019
Locations: Iran (Islamic Republic of);Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/42819