Anderson A A
Department of Clinical Research, May & Baker, Ltd., Essex, U.K.
Sleep. 1987;10 Suppl 1:54-62. doi: 10.1093/sleep/10.suppl_1.54.
The efficacy and tolerance of zopiclone were compared with nitrazepam and placebo in a multicenter double-blind parallel-group study in insomniac patients. Following a 7-day placebo washout period, 99 patients (age range 20 to 69 years) received oral capsules of 7.5 mg zopiclone or 5 mg nitrazepam or placebo for 2 weeks. During the fourth week all patients received placebo treatment. Sleep assessments by the patients showed that, compared with placebo, zopiclone and nitrazepam improved all sleep measures of efficacy from the first night and that effectiveness was maintained throughout treatment. The physicians global assessment of efficacy also favored zopiclone and nitrazepam over placebo treatment. Subjective morning drowsiness during treatment was significantly less for zopiclone than for either nitrazepam or placebo and represents a clear advantage for ambulatory patients. No rebound insomnia was evident during a 7 day post-treatment withdrawal period for either zopiclone or nitrazepam. Tolerance was good for all treatments.
在一项针对失眠患者的多中心双盲平行组研究中,对佐匹克隆与硝西泮及安慰剂的疗效和耐受性进行了比较。经过7天的安慰剂洗脱期后,99名患者(年龄范围为20至69岁)接受了为期2周的口服7.5毫克佐匹克隆胶囊、5毫克硝西泮或安慰剂治疗。在第四周,所有患者均接受安慰剂治疗。患者的睡眠评估显示,与安慰剂相比,佐匹克隆和硝西泮从第一晚起就改善了所有睡眠疗效指标,且在整个治疗过程中疗效得以维持。医生对疗效的总体评估也表明,佐匹克隆和硝西泮比安慰剂治疗更具优势。治疗期间,佐匹克隆导致的主观晨起嗜睡明显少于硝西泮或安慰剂,这对非卧床患者来说是一个明显的优势。在治疗后7天的撤药期内,佐匹克隆或硝西泮均未出现明显的反弹性失眠。所有治疗的耐受性均良好。