ISRCTN04305346已完成未知
Comparative study of efficacy and safety of Structum® and Chondrosulf® in patients with symptomatic osteoarthritis of the knee: a multicentre, randomised, double-blind, double placebo-controlled, parallel group study
Pierre Fabre Research Institute (Institut de Recherche Pierre Fabre) (France)0 个研究点目标入组 837 人开始时间: 2011年4月12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
- 837
研究概览
简要总结
2013 results in https://pubmed.ncbi.nlm.nih.gov/23493263/ (added 18/12/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •Patients aged from 50 to 80 years with symptomatic femorotibial knee OA fulfilling American College of Rheumatology (ACR) criteria for knee OA, with a Kellgren-Lawrence radiological grade II or III, a global pain score greater than or equal to 40 on a 100mm Visual Analogue Scale (VAS) and a Lequesne Index greater than or equal to 7
排除标准
- •1. Isolated symptomatic femoropatellar osteoarthritis of the knee
- •2. Symptomatic hip OA homolateral to the target knee
- •3. Inflammatory, infectious or metabolic arthritis
- •4. Bisphosphonates or strontium ranelate in the 3 months preceding inclusion
- •5. Corticosteroid treatment during the month preceding inclusion
- •6. Intra-articular steroid injection in the 2 months preceding inclusion
- •7. Intra-articular hyaluronic acid in the 6 months preceding inclusion
- •8. Non steroidal anti-inflammatory drugs (NSAIDs) in the 2 days preceding inclusion
- •9. Articular lavage of target knee in the 3 months preceding inclusion
研究者
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