Hazleman B L, Bulgen D Y
Curr Med Res Opin. 1977;5(1):58-63. doi: 10.1185/03007997709108978.
Preliminary results are reported for the first 23 rheumatoid arthritis patients entered in a long-term, double-blind trial to compare the efficacy of flurbiprofen and indomethacin. It was planned that, unless withdrawn, patients from matched pairs received either flurbiprofen (150 mg to 300 mg daily) or indomethacin (75 mg to 150 mg daily) over a minimum period of 6 months, dosage being adjusted to suit exacerbations and remission of disease. In addition to clinical assessments of severity of pain, duration and severity of morning stiffness, joint size and joint score, routine laboratory measurements were carried out, including estimates of serum iron and total iron binding capacity, rheumatoid factor and immunoglobulin levels. This interim report gives the statistical analysis of results from the 17 patients completing from 2 to 4 months of treatment and shows that both drugs were equally effective in controlling disease activity. Withdrawals due to side-effects or exacerbations of disease were similar for both drugs.
报告了首批23名类风湿性关节炎患者参加一项长期双盲试验的初步结果,该试验旨在比较氟比洛芬和吲哚美辛的疗效。计划是,除非退出试验,配对的患者至少在6个月的时间内接受氟比洛芬(每日150毫克至300毫克)或吲哚美辛(每日75毫克至150毫克)治疗,剂量根据疾病的加重和缓解情况进行调整。除了对疼痛严重程度、晨僵持续时间和严重程度、关节大小和关节评分进行临床评估外,还进行了常规实验室测量,包括血清铁和总铁结合能力、类风湿因子和免疫球蛋白水平的测定。这份中期报告给出了17名完成2至4个月治疗的患者结果的统计分析,结果表明两种药物在控制疾病活动方面同样有效。两种药物因副作用或疾病加重而退出试验的情况相似。