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Recruiting NCT06382051

Modifying PEST for Psoriatic Arthritis Screening

Trial Parameters

Condition Plaque Psoriasis
Sponsor Novartis Pharmaceuticals
Study Type INTERVENTIONAL
Phase N/A
Enrollment 502
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2025-01-23
Completion 2026-08-28
Interventions
PEST Screening group

Brief Summary

The purpose of this study is to assess the impact of adding two questions and pictures to the validated PEST on the potential diagnosis of PsA in participants with moderate-to-severe plaque PsO in Canada.

Eligibility Criteria

Key inclusion criteria: 1. Moderate-to-severe plaque PsO patients who are candidates for bDMARDs, as per provincial reimbursement criteria 2. Adult patients at the time of informed consent signature 3. Patients able to understand and willing to comply with protocol requirements, instructions, and restrictions 4. Residents of Canada Key exclusion criteria: 1. Patients who have previously screened positive for PsA through PEST or any other screening method 2. Patients who have been diagnosed with PsA and/or followed by a rheumatologist 3. Patients who have been diagnosed with inflammatory arthritis unrelated to PsA (rheumatoid arthritis, reactive arthritis, enteropathic arthritis, axial spondyloarthritis) 4. Patients treated with a bDMARD for moderate-to-severe plaque PsO or any other medical condition

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