ISRCTN46471047已完成不适用
A multicentre, randomised, controlled, double-blind study, evaluating the efficacy and safety of anakinra in chondrocalcinosis (Étude multicentrique randomisée contrôlée en double-aveugle contre placebo, évaluant l?efficacité et la sécurité de l?anakinra dans la crise de chondrocalcinose articulaire)
niversity Hospital Centre and University of Lausanne (CHUV) (Switzerland)-Service of Rheumatology0 个研究点目标入组 75 人开始时间: 2011年3月18日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 75
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. Informed consent
- •2. Male or female from 18-99 years of age
- •3. Diagnosis of acute calcium pyrophosphate arthritis based on symptoms of acute arthritis and presence of crystals of chronic calcium pyrophosphate dihydrate (CPPD) in the synovial liquid at screening or from a prior analysis
- •4. The start of the acute arthritis should be less than 5 days from inclusion in the study
排除标准
- •1. Corticotherapy orally with dose equivalent of prednisone > 10mg during the 24 h preceding inclusion
- •2. Corticotherapy intramuscular (im) or intravenous (iv) during the 72h preceding inclusion, no matter the dose
- •3. Corticotherapy intra-articularly during 7 days preceding inclusion
- •4. Chronic oral corticotherapy of > 10mg daily
- •5. Uncontrolled respiratory or cardiac failure
- •6. Other causes of acute arthritis
- •7. Active gastric or duodenal ulceration
- •8. Untreated and active malignancy
- •9. Known intolerance or allergy to the study medications
- •10. Active and untreated infection assessed by investigator as a contraindication to study medications
- •11. Other medical problems that are judged prejudicial to the inclusion of the patient in the study by the investigator
- •12. Pregancy or active breast feeding
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