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临床试验/JPRN-UMIN000001026
JPRN-UMIN000001026已完成未知

The effects of high molecular weight sodium hyaluronate on JKOM score and urine CTX-2 concentration -A randomized comparative clinical study with loxoprofen as a control drug- - OA Study

Research Group of Cartilage Metabolism0 个研究点目标入组 300 人开始时间: 2008年2月13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
300

研究概览

简要总结

The early efficacy of IA-HA was not inferior to that of NSAIDs, and the safety of early-phase of IA-HA was superior to that of NSAIDs for patients with knee OA.

研究设计

研究类型
Interventional

入排标准

年龄范围
50years-old 至 80years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • ;Taken glucocorticoids (intra-articular injection, oral use, external use) within previous 4weeks ;Taken NSAIDs (oral, suppository, external) within previous 2weeks ;K-L grade of contralateral knee is 4 ;Secondary OA of the knee (eg. traumatic OA of the knee) ;Patellofemoral OA (K-L grade of more than 3) ;Moderate OA other than knee ;Rheumatoid arthritis ;Having history of total knee replacement or total hip replacement ;Having history of anaphylactoid reaction to sodium hyaluronan or loxoprofene ;Peptic ulcer ;Abnormal dysemia, abnormal hepatic function, abnormal kidney function, abnormal heart function ;Aspirin-induced asthma or its history ;.Inappropriate patients from the doctor's viewpoint

研究者

发起方
Research Group of Cartilage Metabolism

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