Trial Outcomes & Findings for Pruritus in Patients With Chronic Kidney Disease (NCT NCT01727180)

NCT ID: NCT01727180

Last Updated: 2015-03-17

Results Overview

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

Recruitment status

COMPLETED

Target enrollment

108 participants

Primary outcome timeframe

Once at the entry of the study

Results posted on

2015-03-17

Participant Flow

Participant milestones

Participant milestones
Measure
Chronic Kidney Disease
Questionnaire based on the McGill Pain Questionnaire: Interview questionnaire based on the short form of the McGill Pain Questionnaire
Overall Study
STARTED
108
Overall Study
COMPLETED
108
Overall Study
NOT COMPLETED
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Pruritus in Patients With Chronic Kidney Disease

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Chronic Kidney Disease
n=108 Participants
Questionnaire based on the McGill Pain Questionnaire: Interview questionnaire based on the short form of the McGill Pain Questionnaire
Age, Continuous
61.1 years
STANDARD_DEVIATION 12.9 • n=5 Participants
Sex: Female, Male
Female
55 Participants
n=5 Participants
Sex: Female, Male
Male
53 Participants
n=5 Participants

PRIMARY outcome

Timeframe: 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

Outcome measures

Outcome measures
Measure
Chronic Kidney Disease
n=108 Participants
Questionnaire based on the McGill Pain Questionnaire: Interview questionnaire based on the short form of the McGill Pain Questionnaire
Visual Analog Scale (VAS)
3.35 units on a scale
Standard Deviation 2.27

Adverse Events

Chronic Kidney Disease

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Hon-Yen Wu, MD, PHD

Far Eastern Memorial Hospital

Phone: +886-2-8966-7000

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place