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临床试验/NCT01077258
NCT01077258已完成不适用

Effectiveness and Safety of Adalimumab in Patients With Rheumatoid Arthritis in Routine Clinical Practice

AbbVie (prior sponsor, Abbott)303 个研究点 分布在 1 个国家目标入组 4,208 人开始时间: 2004年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
4,208
试验地点
303
主要终点
Change From Baseline in Disease Activity Score (DAS) 28

研究概览

简要总结

Observation of safety, tolerability and effectiveness of adalimumab (Humira) therapy in a large patient collective under everyday clinical conditions over 2 years.

详细描述

Patients with rheumatoid arthritis who started treatment with adalimumab in a normal clinical setting according to the product label were documented. The follow-up observation period was for 2 years and focused on safety information and maintenance of efficacy during a normal clinical setting. Follow-up with participants was via regular office visits at intervals as determined by routine clinical practice or as recommended by national guidelines.

研究设计

研究类型
Observational
观察模型
Case Only
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

  • Moderate to severe active rheumatoid arthritis in adults with insufficient response to disease-modifying antirheumatic drugs, including methotrexate
  • Moderate to severe active rheumatoid arthritis in adults who have not been treated with methotrexate before. In case of incompatibility with methotrexate, Humira can be used as monotherapy

排除标准

  • Hypersensitivity against the drug or one of the other ingredients
  • Active tuberculosis or other severe infections (e.g. sepsis and opportunistic infections)
  • Moderate to severe cardiac insufficiency

结局指标

主要结局

Change From Baseline in Disease Activity Score (DAS) 28

时间窗: Baseline and Months 3, 6, 9, 12, 18, and 24

The Disease Activity Score 28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, the erythrocyte sedimentation rate (ESR), and the patient's assessment of global disease activity (on a visual analog scale \[VAS\] from 0 to 10 cm) are included in the DAS28 score. If the ESR value is missing, the C-reactive protein (CRP) value can be substituted. Scores on the DAS28 range from 0 to 10; higher scores indicate more disease activity. A DAS28 score \>5.1 indicates high disease activity, a DAS28 score \<3.2 indicates low disease activity, and a DAS28 score \<2.6 indicates clinical remission.

Percentage of Participants in DAS28 Remission

时间窗: Months 3, 6, 9, 12, 18, and 24

Clinical remission is defined as a disease activity score (DAS) 28 score of \< 2.6. The DAS28 is a validated index of rheumatoid arthritis disease activity. Twenty-eight tender joint counts, 28 swollen joint counts, the erythrocyte sedimentation rate (ESR), and the patient's assessment of global disease activity (assessed on a visual analog scale \[VAS\] from 0 to 10 cm) are included in the DAS28. If the ESR value is missing, the C-reactive protein (CRP) value can be substituted. Scores on the DAS28 range from 0 to 10; higher scores indicate more disease activity.

次要结局

  • Patients Global Assessment of Disease Activity Over Time(Baseline and Months 3, 6, 9, 12, 18 and 24)
  • Participants Assessment of Fatigue Over Time(Baseline and Month 3, 6, 9, 12, 18, and 24)
  • Percentage of Participants With a Significant Therapeutic Response(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Percentage of Participants With Low, Moderate and High Disease Activity(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Erythrocyte Sedimentation Rate (ESR) Over Time(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • C-Reactive Protein (CRP) Levels Over Time(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Tender Joint Count (TJC) Over Time(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Swollen Joint Count (SJC) Over Time(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Hannover Functional Questionnaire (FFbH) Over Time(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Participants Assessment of Pain Over Time(Baseline and Months 3, 6, 9, 12, 18, and 24)
  • Percentage of Participants With Impairment in Daily Activities(Baseline and Months 3, 6, 9, 18, and 24)
  • Number of Days Missed From Work Due to Rheumatoid Arthritis(Baseline and Months 6, 12, 18, and 24)
  • Percentage of Participants With In-patient Hospitalization(Month 6, 12, 18, and 24)
  • Percentage of Participants on Concomitant Rheumatoid Arthritis and Pain Relief/Anti-inflammatory Medication(Baseline and Months 3, 6, 9, 12, 18, and 24)

研究者

发起方
AbbVie (prior sponsor, Abbott)
申办方类型
Industry
责任方
Sponsor

研究点 (303)

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