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Psoriatic Arthritis Treat to Target vs. Usual Care (PRC-05-2011)

P

Pope Research

Status

Withdrawn

Conditions

Psoriatic Arthritis (PsA)

Treatments

Other: Intensive Care

Study type

Interventional

Funder types

Industry

Identifiers

NCT01692912
PRC-05-2011

Details and patient eligibility

About

Canadian Rheumatologists will be randomized to treat their participants with active Psoriatic Arthritis to a target (disease activity score <2.6), or as per their routine care. The aim of this study is to determine whether treating to a target results in greater disease improvement than treating patients using routine care.

Full description

Canadian Rheumatologists will be randomized to treat their participants with active Psoriatic Arthritis to a target (disease activity score <2.6), or as per their routine care. The aim of this study is to determine whether treating to a target results in greater disease improvement than treating patients using routine care.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Psoriatic Arthritis as diagnosed by a rheumatologist and meeting ACR classification criteria for PsA or CASPAR criteria
  • The subject must provide written informed consent for participation in the study before any study specific procedures are performed
  • Subject has 3 or more SJC on 28 joint count
  • Age >=18

Exclusion criteria

  • Subject has a history of being non-compliant
  • Serious concomitant illnesses that in the investigator's opinion negate ability to optimally treat the patient
  • If treating with TNF inhibitor, positive PPD > 5mm who have not received INH for recommended course or untreated TB (ie CXR evidence of latent infection). Usual screening is in place for standard of care.
  • Pregnancy, breast-feeding or considering pregnancy over the next 12 months

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Intensive Care (IC)
Active Comparator group
Description:
Rheumatologists treating to target of DAS28\<2.6
Treatment:
Other: Intensive Care
Routine Care (RC)
No Intervention group
Description:
Participants treated in the routine manner by their rheumatologist (not treated to the target of DAS28\<2.6)

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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