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Pruritus in Psoriasis

Pruritus in Psoriasis - PruriPso

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00011817
Enrollment
400
Registered
2017-03-22
Start date
2017-01-17
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

L40.0 L29

Interventions

Group 1: Systematic clinical aspects of pruritus are to be systematically analyzed using questionnaires that have never been used in patients with psoriasis: 1. Epidemiological documentation of patien

Sponsors

Klinik für Dermatologie, UKSH Campus Kiel
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: underage patients and /or patients who are unable to consent

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Questinonnaires on pruritus

Countries

Germany

Contacts

Public ContactSascha Gerdes

Klinik für Dermatologie, UKSH Campus Kiel

sgerdes@dermatology.uni-kiel.de0431 500 21151

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026