Medical Affairs and Clinical Research, Ipca Laboratories Ltd, 142 AB, Kandivli Industrial Estate, Kandivli (West), Mumbai 400067, India.
Expert Opin Pharmacother. 2011 May;12(7):1007-15. doi: 10.1517/14656566.2011.566867. Epub 2011 Apr 7.
To demonstrate the clinical noninferiority of the analgesic effect of zaltoprofen (80 mg t.i.d.) compared with diclofenac (50 mg t.i.d.) in active knee osteoarthritis patients.
In this multicentric, double-blind, double-dummy, randomized, parallel-group, comparative study, 213 patients of either sex, aged 40 - 65 years having radiological and clinically confirmed primary knee osteoarthritis were randomized either to zaltoprofen (n = 105) or diclofenac (n = 108) and were followed-up at weeks 1, 2, 3 and 4. The treatment period was preceded by a washout period of 1 week.
Patients in both the zaltoprofen and diclofenac groups exhibited significant improvement (p < 0.001) in pain intensity, functional status and pain relief at each visit from baseline with no statistically significant difference between the two treatment groups. There was no statistically significant difference between the treatment groups for global assessment rating done by the patient and investigator at the end of therapy (p > 0.05) and the proportion of patients who consumed ranitidine (p = 0.135) and paracetamol (p = 0.086) tablets during the treatment period on both the treatment arms. Both the study medications were well tolerated with no incidence of serious adverse events.
This study demonstrated that efficacy and safety of zaltoprofen is clinically noninferior to that of diclofenac.
证明佐来洛芬(tid80mg)与双氯芬酸(tid50mg)相比在治疗活跃性膝骨关节炎患者时的镇痛效果具有临床非劣效性。
在这项多中心、双盲、双模拟、随机、平行组比较研究中,纳入了 213 例年龄在 40-65 岁之间、性别不限、影像学和临床确诊为原发性膝骨关节炎的患者,将其随机分为佐来洛芬组(n=105)或双氯芬酸组(n=108),并在第 1、2、3 和 4 周进行随访。治疗前有 1 周的洗脱期。
佐来洛芬组和双氯芬酸组的患者在每个访视点(从基线开始)的疼痛强度、功能状态和疼痛缓解方面均表现出显著改善(p<0.001),两组之间无统计学差异。在治疗结束时,患者和研究者的整体评估评分(p>0.05)以及在治疗期间使用雷尼替丁(p=0.135)和对乙酰氨基酚(p=0.086)片的患者比例在两组之间无统计学差异。两种研究药物均具有良好的耐受性,无严重不良事件发生。
本研究表明,佐来洛芬的疗效和安全性与双氯芬酸相当。