Trial ID: | L0521 |
Source ID: | IRCT2017102537007N1
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Associated Drug: |
Probiotic
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Title: |
Effect of probiotic in improving laboratory findings in nonalcoholic fatty liver disease
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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: |
--
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Conditions: |
Nonalcoholic fatty liver disease (NAFLD). <br>Fatty (change of) liver, not elsewhere classified;Fatty (change of) liver, not elsewhere classified
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Interventions: |
Intervention 1: In intervention group, two Gerilact tablets 500 mg will be administered daily for 60 days. Intervention 2: In control group, two placebo tablets will be given daily for 60 days.;Treatment - Drugs;Placebo;In intervention group, two Gerilact
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Outcome Measures: |
Lipid profile. Timepoint: Before and at the end of intervention. Method of measurement: with laboratory examination.;Liver function tests. Timepoint: Before and at the end of intervention. Method of measurement: with laboratory examination.;Fatty liver grade. Timepoint: Before and at the end of intervention. Method of measurement: With sonography.nan
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Sponsor/Collaborators: |
Vice chancellor for research, Ardabil University of Medical Sciences
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Gender: |
All
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Age: |
18 yearsno limit
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Phases: |
Not applicable
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Enrollment: |
60
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Study Type: |
interventional
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Study Designs: |
Randomization: Randomized, Blinding: Triple blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
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Start Date: |
12/11/2017
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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/27500
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