The aim of the current study is to evaluate the safety and efficay of Montelukast in treatment of patients with fatty liver disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
56
patients received matching-image placebo once daily at bedtime for 12 weeks.
patients received montelukast (10-mg chewable tablet) once daily at bedtime for 12 weeks.
Faculty of Medicine
Shibīn al Kawm, Menoufia, Egypt
Fibro-scan score
change in liver stiffness measurement (Fibro-scan score)
Time frame: At baseline and after 12 weeks of intervention
Liver Panel
Alanine aminotransferase (ALT) and Aspartate Aminotransferase (AST) will be evaluated in U/L
Time frame: after 12 weeks of intervention
HOMA-IR
Homeostatic Model Assessment of Insulin Resistance
Time frame: after 12 weeks of intervention
8-OHdG
Serum level of 8-OHdG
Time frame: after 12 weeks of intervention
TNF-Alpha
Serum level of TNF-Alpha
Time frame: after 12 weeks of intervention
hyaluronic acid
Serum level of hyaluronic acid
Time frame: after 12 weeks of intervention
TGF-β1
Serum level of TGF-β1
Time frame: after 12 weeks of intervention
Assessment of drugs tolerability: Side effects
Side effects of montelukast
Time frame: after 12 weeks of intervention
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