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OpenTrials
Completed

NCT Number: NCT01727180

Pruritus in Patients With Chronic Kidney Disease

We believe that knowing characteristics of uremic pruritus is the foundation to investigate its pathophysiology and offer better skin care for patients with chronic kidney disease. We therefore conducted this cross-sectional study to evaluate the characteristics of uraemic pruritus.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults older than 20 years old, with CKD stage 3 to 5D, with symptoms of pruritus.

Exclusion criteria

  • Patients who refused to answer the questionnaire or unable to understand the contents of the questionnaire.

Treatment and study plan

Questionnaire based on the McGill Pain Questionnaire

Other

Interview questionnaire based on the short form of the McGill Pain Questionnaire

Primary outcomes

  1. Visual Analog Scale (VAS)

    Time frame: Once at the entry of the study

    A visual analog scale (VAS) measuring the general severity of pruritus was reported from 0 to 10 (0 = no pruritus, 10 = worst pruritus imaginable

Sponsors and collaborators

Lead sponsor

Far Eastern Memorial Hospital

Other

Registry information

Important dates

Study start
2011
Primary completion
2012
Study completion
2013
First posted
Nov 15, 2012
Registry last updated
Mar 17, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.