Viewing Study NCT06382051



Ignite Creation Date: 2024-05-06 @ 8:27 PM
Last Modification Date: 2024-10-26 @ 3:27 PM
Study NCT ID: NCT06382051
Status: NOT_YET_RECRUITING
Last Update Posted: 2024-04-24
First Post: 2024-04-19

Brief Title: Modifying PEST for Psoriatic Arthritis Screening
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: A Multicenter Prospective Study to Evaluate the Impact of Modifying the Validated Psoriasis Epidemiology Screening Tool PEST on the Potential Diagnosis of Psoriatic Arthritis in Adult Patients With Moderate-to-severe Plaque Psoriasis in Canada ScreenX
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: ScreenX
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

Patients will be enrolled in the study for up to 66 days and will be asked to fill-out a PsA screening questionnaire at their first dermatologist visit Patients screening positive for PsA will have a second visit with a rheumatologist where a full PsA diagnosis assessment will be performed A remote end of study EOS visit will be conducted by the dermatologist to document the patients biologic Disease-Modifying Antirheumatic Drugs bDMARDs treatment choice and status
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None