The purpose of this study is to compare the efficacy of etanercept and sulphasalazine in the treatment of Ankylosing Spondylitis.

Official Title

A Randomized, Double-Blind Study Evaluating the Safety and Efficacy of Etanercept and Sulphasalazine in Subjects With Ankylosing Spondylitis

Conditions

Ankylosing Spondylitis

Study Type

Interventional

Study Design

Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study

Further Details

Primary Outcome Measures:

  • To compare the efficacy of etanercept with sulphasalazine in the treatment of ankylosing spondylitis.

Secondary Outcome Measures:

  • To compare the effect of etanercept with sulphasalazine on the quality of life. To evaluate the safety of etanercept.

Study Start

December 2005

Eligibility & Criteria

  • Ages Eligible for Study: 18 Years and above
  • Genders Eligible for Study: Both

Inclusion Criteria:

  • Clinical diagnosis of ankylosing spondylitis
  • Active ankylosing spondylitis

Exclusion Criteria:

  • Complete ankylosis of spine
  • Previous treatment with etanercept

Total Enrolment

525

Contact Details

  • Heidelberg West, Victoria, 3081, Australia; Recruiting
  • Shenton Park, Western Australia, 6000, Australia; Recruiting

Email Trial managers:

  • clintrialparticipation@wyeth.com
  • medinfo@wyeth.com

Please refer to this study by ClinicalTrials.gov identifier: NCT00247962

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