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临床试验/EUCTR2022-003128-42-NL
EUCTR2022-003128-42-NL招募中1 期

REDUCE PMR: Rituximab Effect on Decreasing glUcoCorticoid Exposition in relapsing PolyMyalgia Rheumatica - REDUCE_PMR2

Sint Maartenskliniek0 个研究点目标入组 174 人开始时间: 2022年12月20日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
招募中
入组人数
174

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

  • A clinical diagnoses of PMR according to the 2012 EULAR/ACR classification criteria.
  • Re-emerging PMR symptoms and elevated ESR of CRP levels.
  • Glucocorticoid dose equivalent of prednisolone = 5mg/day.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 174
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 174

排除标准

  • Treatment with systemic immunosuppressants (other than GC) 3 months prior to inclusion
  • (clinical) suspect concomitant giant cell arteritis or other rheumatic inflammatory disease
  • Concomitant conditions that might significantly interfere with evaluation of PMR pain or movement as judged by the investigator
  • Previous hypersensitivity for RTX of contra-indications to RTX
  • Not being able to speak, read or write Dutch

研究者

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