NL-OMON47431已完成4 期
REMission INDuction in very early Rheumatoid Arthritis - REMINDRA
niversitair Medisch Centrum Utrecht0 个研究点目标入组 267 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 267
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •To be eligible to participate in this study, a subject must meet all of the following criteria:
- •- Able and willing to give written informed consent
- •- At least 18 years of age
- •- Fulfilling 2010 ACR/EULAR criteria for RA (Appendix A.)
- •- Patient reported symptom duration (joint stiffness, tenderness, pain, and/or swelling) < 12 months
- •- Naïve for DMARD and biological treatment
- •- DAS28 <=>3.2
- •- Have sufficient knowledge of the Dutch language to be able to comply with the requirements of the study protocol
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •- Having used glucocorticoids < 6 weeks before the baseline visit
- •- Being pregnant (based on anamnesis) or a nursing women or a women of child bearing potential without (adequate) use of contraception
- •- Having any other inflammatory rheumatic disease than RA, except for secondary Sjögren*s syndrome
- •- Having contraindications for the use of MTX/HCQ/methylprednisolone/GOL.
研究者
相似试验
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REMission INDuction in very early Rheumatoid ArthritisEUCTR2015-004858-17-NLniversity Medical Center Utrecht (UMCU)267
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已完成
不适用
Remission Induction in Very Early Rheumatoid Arthritis: a comparison of etanercept plus methotrexate plus steroid with standard therapyISRCTN49682259Record Provided by the NHSTCT Register - 2007 Update - Department of Health20
终止
4 期
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