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Survey on Itch in Outpatients of a University Clinic

Survey on Itch in Outpatients of a University Clinic

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03901443
Enrollment
300
Registered
2019-04-03
Start date
2015-12-09
Completion date
2016-04-30
Last updated
2019-04-08

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

Conditions

Itch

Keywords

itchy skin diseases, itch treatments, pruriception

Brief summary

This study is to investigate the pruriception (i.e. the perception of the character and intensity of itch), the impact of itch on quality of life, the response to itch and the subjective efficacy and preferences of the different treatment options among patients with different skin diseases. Better insights into these aspects might help to optimize itch treatment in clinical Settings.

Interventions

OTHERSurvey on itch

self-administered patient questionnaire regarding the different aspects of itch

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* outpatients suffering from itch

Exclusion criteria

* outpatients (suffering from itch) not willing or able to participate

Design outcomes

Primary

MeasureTime frameDescription
itch intensitysingle time point assessment at baselineQuestions regarding itch perception (NRS 0-10; 0 = no itch, 10 = worst imaginable itch) experienced at the moment, within the last 7 days, within the last month
itch perceptionsingle time point assessment at baselineQuestions regarding situations in which the itch is especially bad (multiple choice options regarding day time, daily situations, season); objective assessment in which respondents are asked to select answers from the choices offered as a list
impact of itch on quality of lifesingle time point assessment at baselineQuestions regarding strength of impact of itch on quality of life (NRS 0-10; 0 = no impact, 10 = extreme)
quality of sleepsingle time point assessment at baselineQuestions regarding sleep disturbance by itch (Does itch disturb the patient's sleep and/or sleep of other persons? (yes/no))
days missing at worksingle time point assessment at baselineApproximate number of days missing at work due to itch within last 6 months
helpfulness of common itch therapiessingle time point assessment at baselineQuestions regarding helpfulness of common itch therapies (NRS 0-10; 0 = no reduction in itch, 10 = complete reduction of itch; additionally free text options to indicate specific creams, tablets or alternative medicine)
preferred treatment optionssingle time point assessment at baselineQuestions regarding preferred treatment options (NRS 0- 10; 0 = unimportant, 10 = most important; including additional free text option)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026