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Retrospective Evaluation of the Radiographic Efficacy of Conventional and Biologic Treatment

Pfizer logo

Pfizer

Status

Completed

Conditions

Rheumatoid Arthritis

Treatments

Drug: DMARDs or Biologics

Study type

Observational

Funder types

Industry

Identifiers

NCT00929357
0881X1-4617

Details and patient eligibility

About

This study involves review and analysis of disease activity in patients with rheumatoid arthritis who where treated with either conventional DMARDs (Disease Modifying Antirheumatic Drugs) or Biologics and have two existing, consecutive radiographs (x-ray images) of hand and feet taken as part of routine treatment monitoring within a time interval of 12 to 36 months.

Enrollment

156 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Secure diagnosis of rheumatoid arthritis
  • Older than 18 years
  • Two consecutive plain radiographs of the hands and feet with a time interval of 12 to 36 months are available. The radiographs are recorded 2003 or later and are in accordance with a defined X-ray protocol.

Exclusion criteria

  • Patients who receive Anakinra, Rituximab or Abatacept

Trial design

156 participants in 2 patient groups

1
Description:
DMARDs
Treatment:
Drug: DMARDs or Biologics
2
Description:
Biologics
Treatment:
Drug: DMARDs or Biologics

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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