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This study is aimed at comparing the efficacy and safety of loxoprofen sodium hydrogel patch (LX-P) with loxoprofen sodium tablet (LX-T) in patients with knee osteoarthritis (OA). One hundred sixty-nine patients were enrolled in a randomized, controlled, double-blind, double-dummy, multicenter, non-inferiority trial of LX-P. Patients were randomly assigned to either LX-P or LX-T groups for a 4-week treatment. The primary efficacy endpoint was the proportion of patients with an overall improvement of ≥50

作者:Rong, Mu;Chun-de, Bao;Zhi-wei, Chen;Yi, Zheng;Guo-chun, Wang;Dong-bao, Zhao;Shao-xian, Hu;Yu-jun, Li;Zeng-wu, Shao;Zhi-yi, Zhang;Wei-guo, Xiao;Weiya, Zhang;Zhan-guo, Li

来源:Clinical rheumatology 2016 年 35卷 1期

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作者:
Rong, Mu;Chun-de, Bao;Zhi-wei, Chen;Yi, Zheng;Guo-chun, Wang;Dong-bao, Zhao;Shao-xian, Hu;Yu-jun, Li;Zeng-wu, Shao;Zhi-yi, Zhang;Wei-guo, Xiao;Weiya, Zhang;Zhan-guo, Li
来源:
Clinical rheumatology 2016 年 35卷 1期
标签:
Hydrogel patch Knee osteoarthritis Loxoprofen sodium Topical application
This study is aimed at comparing the efficacy and safety of loxoprofen sodium hydrogel patch (LX-P) with loxoprofen sodium tablet (LX-T) in patients with knee osteoarthritis (OA). One hundred sixty-nine patients were enrolled in a randomized, controlled, double-blind, double-dummy, multicenter, non-inferiority trial of LX-P. Patients were randomly assigned to either LX-P or LX-T groups for a 4-week treatment. The primary efficacy endpoint was the proportion of patients with an overall improvement of ≥50