Development of a questionnaire for the assessment of Itch-Free-Days

• Conditions: L28.1; L29.8; Prurigo nodularis; Other pruritus

• Registration Number: DRKS00010255
• Lead Sponsor: Kompetenzzentrum chronischer Pruritus (KCP) und Klinik für Hautkrankheiten Universitätsklinikum Münster

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2016-03-15
• Study Start: 2016-04-11
• Results First Posted: 2017-09-27
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 209

Inclusion Criteria

Pruritus intensity of at least NRS 3 (numeric rating scale 0-10)

Exclusion Criteria

Pregnancy, breast feeding, Drug consumption, prescription drug abuse, Topical application of steroids, calcineurin inhibitors within the past week, Cutaneous infections, systemic therapy unchanged

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Validation of the IFD (Itch free days) questionnaire

Secondary Outcome Measures

Name	Time	Method
Determination of a score for itch free days