About this trial
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.
Eligibility criteria
Qualifiers
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.
Disqualifiers
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)
Trial design
Treatments tested in this trial
- Data collection