Camus J P, Prier A
Nouv Presse Med. 1982 Aug 28;11(33):2481-3.
One hundred ninety-five patients suffering from active rheumatoid arthritis were included in a two-week double blind multicentric study, whose purpose was to compare the efficacy and tolerance of a daily dose of 600 mg of pirprofen to that of 1200 mg and the placebo. The results show that there is a dose-effect relationship of definite clinical interest. Thus, the investigators judged the clinical results satisfactory in 60% of the patients in the 1200 mg group (400 mg t.i.d.) 44% of those in the 600 mg group and 36% of those on placebo. The difference is statistically significant (p less than 0.05). Side effects, primarily digestive, were noted in 34% of patients receiving 1200 mg/day, 15% of 600 mg/day and 32% placebo. 2 patients in the 1200 mg group interrupted their treatment for gastralgia and 1 patient on placebo for palpitations.
195名活动性类风湿关节炎患者被纳入一项为期两周的双盲多中心研究,该研究旨在比较每日剂量600毫克吡洛芬与1200毫克吡洛芬及安慰剂的疗效和耐受性。结果表明,存在具有明确临床意义的剂量效应关系。因此,研究人员判定,1200毫克组(每日三次,每次400毫克)60%的患者、600毫克组44%的患者以及安慰剂组36%的患者临床结果令人满意。差异具有统计学意义(p小于0.05)。主要为消化系统的副作用在接受1200毫克/天的患者中占34%,600毫克/天的患者中占15%,安慰剂组中占32%。1200毫克组有2名患者因胃痛中断治疗,安慰剂组有1名患者因心悸中断治疗。