Validation of novel instrument for pruritus documentation

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00009902

Enrollment

200

Registered

2016-03-09

Start date

2014-09-01

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

itching L29.9

Interventions

Group 1: 40 patients initially receive the instruments used in our routine on paper: pruritus intensity (VAS, VRS, NRS), dynamic score, life quality via DLQI, ItchyQol and the Anxiety and Depression q

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: chronic pruritus different origins

Exclusion criteria

Exclusion criteria: Pregnancy and breast feeding

Design outcomes

Primary

Measure	Time frame
Determination of the congruent validity of the novel instruments for pruritus documentation	—

Secondary

Measure	Time frame
Determination of the interitem validity, retest-reliability of the instruments	—

Countries

Germany, Poland, United States

Contacts

Public ContactEmil Rose Burnett

Klinik für Hautkrankheiten und Kompetenzzentrum Chronischer Pruritus

juckreizambulanz@ukmuenster.de0251 83 57470

Outcome results

None listed

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