Pruritus in Psoriasis

• Conditions: L40.0; L29; Psoriasis vulgaris; Pruritus

• Registration Number: DRKS00011817
• Lead Sponsor: Klinik für Dermatologie, UKSH Campus Kiel

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-03-22
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 329

Inclusion Criteria

Patients above 18 years who have Psoriasis and are able to consent.

Exclusion Criteria

underage patients and /or patients who are unable to consent

Study & Design

• Study Type: observational
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The aim of the project is the systematic characterization of pruritus in patients with psoriasis. The following questionnaires are used at the time of examination: Dermatological Life Quality Index (DLQI), Itch-Free Days (IFD Questionnaire), Hospital Anxiety and Depression Scale (HADS), Neuro_Derm Questionnaire Psoriasis, Quality of Life Questionnaires (ItchQoL), Pruritus Quality of Life Questionnaire (5PLQ) , Pain questionnaire (PAIN-Detect).

Secondary Outcome Measures

Name	Time	Method
Questinonnaires on pruritus