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NCT02530268Enrolling by invitation

The Corrona Psoriatic Arthritis and Spondyloarthritis (PsA-SpA) Registry

Corrona Psoriatic Arthritis and Spondyloarthritis (PsA-SpA) Registry

Source: ClinicalTrials.gov · Last updated 9 Feb 2026

Brief summary (registry, in English)

This prospective, non-interventional, research registry is designed to study the comparative effectiveness and comparative safety of approved treatments for PsA-SpA in a cohort of patients cared for by rheumatologists across North America. Secondary objectives include analyzing the epidemiology and natural history of the disease, its comorbidities, and current treatment practices.

Status (registry)
Enrolling by invitation
Study type
Observational
Enrollment
5000 (estimated)
First submitted
1 May 2015
Start date
Mar 2013
Primary completion date
Dec 2100
Lead sponsor
CorEvitas
NCT number
NCT02530268

What you commit to

  • Study type: Observational
  • Planned participants: 5000
  • From Mar 2013 to the primary completion date, Dec 2100
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participating in or planning to participate in a clinical trial with an interventional research study of a non-marketed or marketed investigational drug (e.g. phase I-IV clinical drug trial, post marketing study or registry study where drug is being provided). Of note, concurrent participation in another observational registry study is not excluded. ∆
    • Once clinical trial participation has ended, a patient is permitted to enroll in the registry if they satisfy the eligibility requirements at the time of enrollment. If the patient participated in the PsA-SpA registry and was exited to join a clinical trial, the patient cannot be re-enrolled in the PsA-SpA registry after clinical trial participation has ended.
    • Patients switching from an originator biologic to a biosimilar satisfy the enrollment eligibility requirement.

Other illness

  • Diagnosed with rheumatoid arthritis, systemic lupus erythematosus, or any other form of autoimmune inflammatory arthritis.

Other

  • The patient must not be:

Who the study is looking for

  • The patient must be:
  • One of the following:
    • Diagnosed with psoriatic arthritis (PsA) and initiating (prescribed or starting) an eligible medication† for the treatment of PsA at the enrollment visit.
    • Meet the ASAS criteria for axial spondyloarthritis (AxSpA), including radiographic or non-radiographic, and initiating (prescribed or starting) an eligible biologic for the treatment of AxSpA at the enrollment visit.
    • Meet the modified New York classification criteria for ankylosing spondylitis (AS) and initiating (prescribed or starting) an eligible biologic for the treatment of AS at the enrollment visit
  • At least 18 years of age or older
  • Able and willing to provide written consent

Criteria the registry did not label

  • To be eligible for enrollment into the Corrona PsA-SpA Registry, a patient must satisfy all of the inclusion criteria and none of the exclusion criteria listed below.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.