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NCT01727180 Clinical Trial

Pruritus in Patients With Chronic Kidney Disease

Kidney Failure, Chronic Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01727180
Other study ID # 100047-E
Secondary ID
Status Completed
Phase N/A
First received November 12, 2012
Last updated March 4, 2015
Start date June 2011
Est. completion date December 2013

Study information
Verified date March 2015
Source Far Eastern Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Institutional Review Board
Study type Observational

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 108
Est. completion date December 2013
Est. primary completion date June 2012
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility 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.

Study Design

Observational Model: Case-Only, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

Intervention

Other:
• Questionnaire based on the McGill Pain Questionnaire
Interview questionnaire based on the short form of the McGill Pain Questionnaire

Locations
Country Name City State
Taiwan Far Eastern Memorial Hospital New Taipei City

Sponsors (1)
Lead Sponsor Collaborator
Far Eastern Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome
Type Measure Description Time frame Safety issue
Primary Visual Analog Scale (VAS) A visual analog scale (VAS) measuring the general severity of pruritus was reported from 0 to 10 (0 = no pruritus, 10 = worst pruritus imaginable Once at the entry of the study No
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