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临床试验/jRCT1030250036
jRCT1030250036已完成不适用

Epidemiology and Treatment Trends of Rheumatoid Arthritis with Dementia in Japan: A Nationwide Claims Database Study

Eisai Co., Ltd.,0 个研究点目标入组 450,000 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
450,000
主要终点
prevalence of dementia

研究概览

简要总结

暂无简介。

研究设计

研究类型
Other
分配方式
Non-randomized Controlled Trial
干预模型
Single Assignment
主要目的
Other
盲法
Open(masking Not Used)

入排标准

年龄范围
65age old over 至 No limit(—)
性别
All

入选标准

  • Patients had to fulfill all of the following criteria to be included in the study: aged >=65 years at the time of RA diagnosis between 1 January 2015 and 31 December 2023 (ICD-10 codes M05, M060, M062, M063, M068, M069, excluding RS3PE syndrome [standard injury code: 8844120], wrist deformity [standard injury code: 8845190], and ulnar deviation [standard injury code: 8845158]); with at least one prescription for a DMARD or oral glucocorticoid within 1 year of the first RA diagnosis; and with a record of data in the DeSC database for at least 180 days prior to the index date.

排除标准

  • No exclusion criteria were set for the primary study endpoint. For secondary endpoints, individuals who lacked prescription records for DMARDs or oral corticosteroids within 1 year of the index date were excluded.

结局指标

主要结局

prevalence of dementia

时间窗: 2015-2023

The prevalence of dementia in all patients with RA aged >=65 years

次要结局

  • annual incidence of dementia in patients with RA aged 65-74 and >=75 years(annual)
  • status of DMARD prescriptions in patients with RA aged 65-74 and >=75 years who developed dementia
  • survival time analysis for new prescriptions or increased doses of oral glucocorticoids in patients aged 65-74 and >=75 years who developed dementia

研究者

发起方
Eisai Co., Ltd.,

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