Clinical Trial Details

Trial ID: L0610
Source ID: IRCT2015042020951N2
Associated Drug: H.pylori eradication
Title: The study of treatment of Helicobacter Pylori in improvement of non-alcoholic fatty liver disease
Acronym: --
Status: Not Recruiting
Study Results: No Results Available
Results: --
Conditions: Condition 1: Nonalcoholic fatty liver disease. Condition 2: Helicobacter pylori infection. <br>Fatty (change of) liver, not elsewhere classified <br>Helicobacter pylori [H.pylori] as the cause of diseases classified to other chapters;Fatty (change of) liv
Interventions: Intervention 1: Case group: treatment of Helicobacter Pylori with omeprazole (20 mg bid), amoxicilin (1gr bid), and clarithromycin (500 mg bid) orally for 2 weeks. Intervention 2: Control group: will receive only symptomatic therapy, if indicated; for exa
Outcome Measures: Aspartate aminotransferase. Timepoint: at the start and end of the study. Method of measurement: by clinical labratory.;Alanine aminotransferase. Timepoint: at the start and end of the study. Method of measurement: by clinical labratory.;Sonographic indices of fatty liver disease. Timepoint: at the start and end of the study. Method of measurement: by a trained sonologist.nan
Sponsor/Collaborators: research department of medical college of QUMS
Gender: All
Age: 18 years60 years
Phases: Not applicable
Enrollment: 30
Study Type: interventional
Study Designs: Randomization: Randomized, Blinding: Not blinded, Placebo: Used, Assignment: Parallel, Purpose: Treatment.
Start Date: 12/05/2015
Completion Date: --
Results First Posted: --
Last Update Posted: 22 February 2018
Locations: Iran (Islamic Republic of)
URL: http://en.irct.ir/trial/18489