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临床试验/ISRCTN16316564
ISRCTN16316564暂停未知

Telemonitoring of patient administered index RAPID3 to deliver NICE compliant treat-to-target strategy in early rheumatoid arthritis

Royal National Orthopaedic Hospital0 个研究点目标入组 30 人开始时间: 2019年2月12日最近更新:
适应症

试验速览

阶段
未知
状态
暂停
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Aged 18 or above
  • 2. Newly diagnosed RA fulfilling ACR/EULAR 2010 criteria for the diagnosis

排除标准

  • 1. Age < 18 years
  • 2. Unable or unwilling to give informed consent
  • 3. Women pregnant, breast feeding or at risk of conceiving
  • 4. Prior treatment with DMARDs
  • 5. Contraindications to DMARD therapy such as recurrent infections, pancytopenia, LFT derangement
  • 6. Mental incapacity to participate in research study, complete RAPID3 and other patient-based study assessments
  • 7. Inability of patient to complete web-based RAPID3 due to the lack of internet facilities or knowledge required to use internet
  • 8. Currently participating or recently participated in another interventional trial

研究者

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