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临床试验/NCT01438892
NCT01438892已完成不适用

Impact Of RA Therapy Compliance On Patient-Reported Outcomes

Pfizer0 个研究点目标入组 396 人开始时间: 2012年2月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
396
主要终点
HAQ

研究概览

简要总结

Several observational studies have evaluated the comparative treatment costs associated with each agent, particularly those within the anti-TNF class, but few have evaluated the impact of therapy compliance, persistence, treatment patterns on patient reported outcomes, healthcare utilization and costs, using a provider database. This study is designed to fill in this information gap.

详细描述

Cohort observational

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults with moderate to severe RA who are currently using a DMARD

排除标准

  • Psoriatic Arthritis (PsA), Psoriasis (PsO), SSystemic Lupus Erythematosus (SLE), Non-Disease modifying anti-rheumatic disease (non-DMARD) use

研究组 & 干预措施

tDMARDs Group

traditional DMARDs

干预措施: tDMARDs (Drug)

Biologics group

Biologics used in RA

干预措施: biodmards (Drug)

结局指标

主要结局

HAQ

时间窗: 12 months

36-Item Short-Form Health Survey (SF-36)

时间窗: 12 months

次要结局

  • Compliance(12 months)

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

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