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PSOREAL - Managing PSOriasis in the REAL World

Completed
Conditions
Psoriasis Vulgaris
Interventions
Registration Number
NCT02935582
Lead Sponsor
LEO Pharma
Brief Summary

Multinational real-life study of current psoriasis treatment strategies, topical treatment patterns and treatment outcomes of these treatments, including the newly introduced calcipotriol/betamethasone dipropionate aerosol foam fixed combination product Enstilar® (calcipotriol/betamethasone dipropionate).

Detailed Description

This multinational study aims to describe current treatment patterns and outcomes in the diversity of the real life setting: local differences in access to drugs and current treatment practices, and regional cultural differences, covering adult patients of all backgrounds, sex, socio-economic standing, health background, comorbidity and co-medication. A total of around 400 real-life prescribers in 3-8 countries are expected to participate over the years, with each country contributing data to the study for around 2 years, starting data collection within the first year after local market introduction of Enstilar®.

The real-life prescribing and utilization patterns of topical prescription products approved for treatment of psoriasis vulgaris in the individual participating countries will be mapped and performance of the products in real life will be investigated based primarily on baseline data from investigators and patient reported data contributed by the individual patient for 1 year. Patients are expected to enter data on their electronic device at baseline and at times of treatment changes and other key events, and investigators are expected to contribute data after each contact with the patient.

Patients will be approached for informed consent to participate in the study after their individual treatment plan has been decided. The study aims to include two patients on other topical treatment for every patient planned to receive Enstilar® in order to ensure a sufficient sample of Enstilar® treated patients to capture the diversity of real-life prescription patterns in patients not on Enstilar®, and to allow for sufficiently powered comparisons between Enstilar® and other real-world treatment strategies. A systematic approach will be used to select eligible patients to be approached for study participation in order to minimize selection bias and control seasonal variations.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1214
Inclusion Criteria
  • Adult age
  • Psoriasis vulgaris
  • Plaques on the body (trunk and/or extremities) of at least mild severity at time of inclusion
  • Decision to prescribe a topical psoriasis treatment for body use where the prescription is NOT a routine renewal of the prescription of an ongoing therapy
  • Signed and dated informed consent
  • Willingness and ability to enter personal disease and treatment information onto a secure webpage during the one year individual study period, using their existing access to a PC or electronic device and a personal access code.
Exclusion Criteria
  • Participation in the active treatment phase of a clinical trial
  • Previous enrollment in the study

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Enstilar®Enstilar® aerosol foamPatients for whom a new treatment strategy has been decided which involves start of topical treatment with Enstilar® according to the current local labelling
Other topicalOther topicalPatients for whom a new treatment strategy has been decided which involves start of topical treatment not including Enstilar®
Primary Outcome Measures
NameTimeMethod
PaGA4 weeks

Patient reported Global Assessment

Itch1 week

Itch dimension of Psoriasis Symptom Inventory (PSI) questionnaire

Switch1 year

Time to switch of topical treatment strategy

Flare-up1 year

Time to first flare-up after initial treatment completion

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Psoriasis association in Stockholm region

🇸🇪

Stockholm, Sweden

Dr. Chih-Ho Hong Medical Inc.

🇨🇦

Surrey, British Columbia, Canada

Layton Medical Centre

🇬🇧

Blackpool, Lancashire, United Kingdom

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