| Trial ID: | L0541 |
| Source ID: | IRCT2017060212789N14
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| Associated Drug: |
Rosvastatin
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| Title: |
The effect of Rosvastatin on steatosis and fibrosis in patients with non-alcoholic fatty liver disease: a randomized controlled clinical trial study
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| Acronym: |
--
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| Status: |
Not Recruiting
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| Study Results: |
No Results Available
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| Results: |
--
|
| Conditions: |
Nonalcoholic fatty liver disease (NAFLD). <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
|
| Interventions: |
Intervention 1: Control Group: patients received placebo daily plus standard treatment for fatty liver disease. Intervention 2: Intervention Group: patients received 10 mg Rosvastatin daily plus standard treatment for fatty liver disease.;Treatment - Drug
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| Outcome Measures: |
Steatosis of liver. Timepoint: Before intervention, six month after intervention. Method of measurement: Fibroscan.;Fibrosis of liver. Timepoint: Before intervention, six month after intervention. Method of measurement: Fibroscan.ALT. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;AST. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;LDL. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;HDL. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Triglyceride. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Bilirubin. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Blood urea. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.;Blood creatinine. Timepoint: Before intervention, six month after intervention. Method of measurement: Blood examination.
|
| Sponsor/Collaborators: |
Vice Chancellor for Research of Kurdistan University of Medical Sciences
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| Gender: |
All
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| Age: |
20 years70 years
|
| Phases: |
Phase 3
|
| Enrollment: |
40
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| Study Type: |
interventional
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| Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
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| Start Date: |
12/06/2017
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| Completion Date: |
--
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| Results First Posted: |
--
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| Last Update Posted: |
22 February 2018
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| Locations: |
Iran (Islamic Republic of)
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| URL: |
http://en.irct.ir/trial/12802
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