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临床试验/NCT03703817
NCT03703817已完成不适用

TREATMENT SATISFACTION COMPARISON IN RHEUMATOID ARTHRITIS PATIENTS BETWEEN TOFACITINIB CITRATE AND ADALIMUMAB, EACH USED IN RHEUMATOID ARTHRITIS TREATMENT

Pfizer23 个研究点 分布在 1 个国家目标入组 421 人开始时间: 2018年7月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
Pfizer
入组人数
421
试验地点
23
主要终点
Treatment Satisfaction Questionnaire for Medication (TSQM) Version 1.4

研究概览

简要总结

RA satisfaction OR: This study aim to compare treatment satisfaction and quality of life between patients who have been using tofacitinib citrate and patients who have been using adalimumab for 6 months or more and less than 2 year in RA treatment of rheumatoid arthritis.

详细描述

RA satisfaction OR: This study aim to compare treatment satisfaction and quality of life between patients who have been using tofacitinib citrate and patients who have been using adalimumab for 6 months or more and less than 2 year in RA treatment of rheumatoid arthritis.

Study design: Non-interventional, multi-centers, cross-sectional study

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

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

入选标准

  • Patients aged 19 years or older
  • Patients diagnosed with RA
  • Treatment groups:
  • Tofacitinib citrate users: Patients currently on treatment with tofacitinib citrate in RA therapy for 6 months or more 2) Adalimumab users: Patients currently on treatment with adalimumab in the RA therapy for 6 months or more
  • Reading and writing with enough proficiency to complete assessment instruments in Korean

排除标准

  • Patients currently on tofacitinib citrate or adalimumab for 2 year or more
  • Patients taking Azathioprine and cyclosporine
  • Patients participating in other drug interventional study
  • Patients who have been treated with bDMARDs except Rheumatoid arthritis.

结局指标

主要结局

Treatment Satisfaction Questionnaire for Medication (TSQM) Version 1.4

时间窗: Day 1 (during approximately 20 months of data collection and observation)

TSQM version 1.4: participant rated 14 items with 4 domains. Scores for item 1 to 3, 9 to 11 and 14 ranged from 1=extremely dissatisfied to 7=extremely satisfied. Items 5 to 8, 12, 13 ranged from 1=extremely dissatisfied to 5=not at all dissatisfied. Item 4 was scored as: 0=No, 1=Yes. Effectiveness measured as (\[{sum of item 1 to 3} - 3\]/18)\*100; if 1 question (Q) was missing: (\[{sum of item 1 to 3} -2\]/12)\*100. Side-effect measured as if item 4=No, score=100; if not then (\[{sum of item 5 to 8} -4\]/16)\*100; if 1 Q was missing: (\[{sum of item 5 to 8} -3\]/12)\*100. Convenience measured as (\[{sum of item 9 to 11} -3\]/18)\*100; if 1 Q was missing: (\[{sum of item 9 to 11} - 2\]/12)\*100. Global satisfaction as (\[{sum of item 12 to 14} -3\]/14)\*100; if item 12 or 13 was missing: (\[{sum of item 12 to 14} -2\]/10)\*100; if item 14 was missing: (\[{sum of item 12 and 13} -2\]/8)\*100. All domains had scale of 0 (no satisfaction) to 100 (best level of satisfaction), higher score=greater satisfaction.

次要结局

  • European Quality of Life-Visual Analogue Scale (EQ-VAS) Score(Day 1 (during approximately 20 months of data collection and observation))
  • European Quality of Life-5 Dimensions-3 Level (EQ-5D-3L) Index Score(Day 1 (during approximately 20 months of data collection and observation))

研究者

发起方
Pfizer
申办方类型
Industry
责任方
Sponsor

研究点 (23)

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