Montelukast for Treatment of Uremic Pruritus

Renal Insufficiency, Chronic Clinical Trial

Official title: Assessment of Montelukast Efficacy in the Treatment of Refractive Uremic Pruritus

Status Completed

Clinical Trial Summary

In this study hemodialysis patients that underwent dialysis thrice weekly screen for uremic pruritus and 80 patients that at least have refractive pruritus that lead to sleep and daily activity disorders enroll in this study. These patients should have at least a course of therapy without proper response. After proper informing patients and taking testimonial patients enter to study. Then patients randomized in case and control group. In case group, patients took montelukast 10 milligram daily and in control group took placebo for 30 days. Other antipruritic or antiinflammatory medication has been stopped one week prior to starting treatment. Calcium, phosphorous, urea, creatinine, highly sensitive CRP (hsCRP), Parathyroid Hormone (PTH), hemoglobin and kt/V were measured at beginning and at end of study. pruritus severity assessed by Detailed Pruritus Score that introduced by Duo and Visual Analogue Score in beginning and at end of study in both group. Sleep disorder score and its severity added to crude score at beginning and end of study and change of measures analyzed.

Clinical Trial Description

Montelukast is an antileukotrien receptor antagonist that seems to be effective as an antipruritic medication via blocking inflammatory pathways. ;

Related Conditions & MeSH terms

• Pruritus
• Renal Insufficiency
• Renal Insufficiency, Chronic

• NCT number: NCT02559388
• Study type: Interventional
• Source: Shiraz University of Medical Sciences
• Status: Completed
• Phase: N/A
• Start date: April 2015
• Completion date: August 2015