Prurigo Nodularis (PN)
Conditions
Interventions
Test group:Non-interventional
Sponsors
The First Hospital of China Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Patients aged 18 years or older at the time of informed consent. 2. Physician decision to treat the patient with dupilumab for prurigo nodularis (according to the country-specific prescribing information) made prior to and independently of the patient’s participation in the study. 3. Patients able to understand and complete study-related questionnaires. 4. Patients provide voluntary informed consent to participate in the study before inclusion in the study.
Exclusion criteria
Exclusion criteria: 1. Patients who have a contraindication to dupilumab according to the country-specific prescribing information label. 2. Any condition that, in the opinion of the Investigator, may interfere with the patient’s ability to participate in the study, such as short life expectancy, substance abuse, severe cognitive impairment, or other comorbidities that can predictably prevent the patient from completing the schedule of visits and assessments. 3. Patients currently participating in any interventional clinical trial. 4. Prior use of dupilumab within 6 months of the screening visit, or within 6 months of the baseline visit if screening and baseline occur on the same day.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To characterize real-world use pattern of dupilumab for prurigo nodularis (PN) ; | — |
Secondary
| Measure | Time frame |
|---|---|
| To characterize the medical history, socio-demographic, disease characteristics, and prior or concomitant medication in dupilumab treated PN patients;To evaluate the long-term real-world effectiveness of dupilumab for the treatment of PN;To collect safety data on study participants ; | — |
Countries
China
Contacts
Public ContactXinghua Gao
The First Hospital of China Medical University
Outcome results
None listed