ISRCTN15819795已完成未知
Effect of anakinra (soluble interleukin-1 receptor antagonist) as combination therapy: second UK combination therapy in early rheumatoid arthritis
King's College London (UK)0 个研究点目标入组 158 人开始时间: 2007年1月26日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 158
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
- 性别
- All
入选标准
- •1. RA by the 1987 criteria of the American College of Rheumatology
- •2. Disease duration of less than 12 months
- •3. The clinical need for treatment with a Slow Acting Anti-Rheumatic Drug (SAARD) as shown by evidence of active RA with three out of the following four criteria:
- •3.1. At least three swollen joints on a 28 joint score
- •3.2. At least six tender joints on a 28 joint score
- •3.3. At least 45 minutes morning stiffness
- •3.4. Erythrocyte Sedimentation Rate (ESR) of at least 28 mm/h
- •4. Patients must be willing and able to give informed consent
- •5. Aged at least 18
排除标准
- •1. Other forms of inflammatory arthritis (e.g. psoriatic arthritis, systemic lupus erythematosus)
- •2. Previous treatment with methotrexate
- •3. Contraindications or known intolerance to any of the drugs allowed on this trial (including Non Steroidal Anti-Inflammatory Drugs [NSAID], Steroids and Disease Modifying Anti-Rheumatic Drugs [DMARDs])
- •4. Other serious medical disorders (e.g. hepatic failure, gout, cardiac failure, tuberculosis, current malignant disease)
- •5. Any acute or chronic infection, including pneumonias
- •6. Females of child bearing and males of child fathering potential who are not taking adequate contraceptive protection
- •7. Neutrophil count less than 1.5 x 10^12/dl or platelet count less than 100 x 10^12/dl
- •8. Abnormal liver function test (gamma-Glutamyl Transferase [gGT] more than three times or Aspartate aminotransferase [AST]/Alanine aminotransferase [ALT] more than two times upper limit of normal)
- •9. Abnormal chest x-ray results
- •10. Patients with severe renal impairment (creatinine clearance less than 30 ml/min). Patients with a creatinine clearance between 30 and 50 ml/min can be entered into the trial but must be closely monitored
- •11. Patients taking low-dosage oral steroids for the treatment of RA. Patients taking a short-course of oral steroids for another condition may be included providing the daily dosage of steroids is less than 20 mg total
研究者
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