Trial ID: | L0882 |
Source ID: | IRCT2014010715879N3
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Associated Drug: |
Lactulose
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Title: |
Study of lactulose effects in the treatment of non alcoholic fatty liver disease in comparison with vitamin E: A randomized, clinical trial
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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: |
Non alcoholic fatty liver disease. <br>Non alcoholic fatty liver disease;Non alcoholic fatty liver disease
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Interventions: |
Intervention 1: Patients in the intervention group receive 20- 30cc lactulose daily for one month. Lactulose syrup (or Laxilose??, 10 g lactulose/15 mL, Alborzdaru) is a synthetic sugar used to treat constipation. In the colon, lactulose is metabolized p
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Outcome Measures: |
Liver size. Timepoint: Baseline and one month after starting the study. Method of measurement: Ultrasound sonography.Intestinal probiotic count. Timepoint: Baseline and one month after starting the study. Method of measurement: Pour plate technique.;Drug complications. Timepoint: One month after starting the study. Method of measurement: Ask the patient.
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Sponsor/Collaborators: |
Vice chancellor for research, Tabriz university of medical sciences
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Gender: |
All
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Age: |
30 years70 years
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Phases: |
Not applicable
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Enrollment: |
40
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Study Type: |
interventional
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Study Designs: |
Randomization: Randomized, Blinding: Double blinded, Placebo: Not used, Assignment: Parallel, Purpose: Treatment, Other design features: Patients will be randomly divided into two groups using the software Randlist 1.2.
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Start Date: |
08/02/2015
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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/15013
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