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
|