跳至主要内容
临床试验/DRKS00021182
DRKS00021182招募中不适用

Evaluation of bone mineral density and bone metabolism during treatment with the januskinaseinhibitor upadacitinib in patients with rheumatoid arthritis

Campus Kerckhoff der Jusuts-Liebig-Universität Gießen, Abteilung für Rheumatologie, Immunologie, Osteologie und Physikalische Medizin0 个研究点目标入组 60 人开始时间: 2020年3月26日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 99 Years(—)
性别
All

入选标准

  • Patients > 18 years with moderate to severe active rheumatoid arthritis who are going to receive treatment with upadacitinib [Rinvoq®]. The indication for treatment with upadacitinib needs to be given by the treating rheumatologist. Only patients with RA fulfilling the ACR/EULAR classification criteria are eligible.

排除标准

  • Contraindications to treatment with upadacitinib [Rinvoq®].
  • Incompatible language barriers
  • Missing consent
  • During study: inadherence to pharmacological treatment

研究者

发起方
Campus Kerckhoff der Jusuts-Liebig-Universität Gießen, Abteilung für Rheumatologie, Immunologie, Osteologie und Physikalische Medizin

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