Swiss Itch Registry

Recruiting now

Conditions studied: Pruritus

In brief

This project is to develop a national registry for CP patients. Patients admitted to this registry will be examined and documented with PROs, physician-based assessments, blood tests, 3D photodocumentation and, if indicated, by skin biopsies, neurophysiological testing and radiological imaging at defined timepoints. The data collection will allow deepened insights into patient needs, different mechanisms and courses of pruritic conditions, treatment outcomes and treatment-related safety issues. In addition, the collection of clinical, biological and image-based data may be used for retrospective analyses.

Key facts

Study ID

NCT06120907

Run by

University Hospital, Basel, Switzerland

People needed

100

Starts

2023-10-18

Expected to finish

2033-10-01

Last updated by the study team

2024-12-13

Who can join

Age: 14 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age ≥ 14 years.
• Written informed consent of the patient.
• Diagnosis of CP irrespective of the International Forum for the Study of Itch (IFSI) group (I-III) and/or underlying cause (according to the judgment of the investigator).
• A Numerical Rating Scale (NRS) score of min. ≥ 4 within the last 7 days.
• Sufficient language skills (in the languages which the patient information and the consent form is available) to provide informed consent.

You may not qualify if…

• Any medical or psychological condition in the treating physician's opinion, which may prevent the patient in registry participation
• Lack of informed consent for registry participation.
• Refusal to complete Patient Reported Outcomes (PROs)

Where it is running

• Department of Dermatology, University Hospital Basel — Basel, Switzerland (enrolling)

Full record on ClinicalTrials.gov

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