Evaluation of the Condition of Rheumatoid Arthritis After Treatment

Overview

To examine the safety and effectiveness after Xeljanz treatment in rheumatoid arthritis patients

Full Title of Study: “Evaluation of the Condition After Xeljanz Treatment in Rheumatoid Arthritis Patients”

Study Type

  • Study Type: Interventional
  • Study Design
    • Allocation: N/A
    • Intervention Model: Single Group Assignment
    • Primary Purpose: Treatment
    • Masking: None (Open Label)
  • Study Primary Completion Date: April 2016

Interventions

  • Drug: The effectiveness of Xeljanz in rheumatoid arthritis patients

Arms, Groups and Cohorts

  • Experimental: The condition of rheumatoid arthritis

Clinical Trial Outcome Measures

Primary Measures

  • Change from baseline of clinical evaluation in rheumatoid arthritis
    • Time Frame: Every month
    • DAS28, SDAI, Blood testing, Plain radiograph, and Ultrasound will be performed.

Secondary Measures

  • Number of participants with adverse events
    • Time Frame: Every month

Participating in This Clinical Trial

Inclusion Criteria

  • Rheumatoid arthritis Exclusion Criteria:

  • Other connective tissue disease

Gender Eligibility: All

Minimum Age: 20 Years

Maximum Age: 90 Years

Are Healthy Volunteers Accepted: Accepts Healthy Volunteers

Investigator Details

  • Lead Sponsor
    • Shinshu University
  • Collaborator
    • Showa Inan General Hospital
  • Provider of Information About this Clinical Study
    • Principal Investigator: Yukio Nakamura, Assistant Professor – Shinshu University
  • Overall Contact(s)
    • Yukio Nakamura, MD, PhD, yxn14@aol.jp

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