Cooper A J, Magnus R V
Pharmatherapeutica. 1980;2(5):317-22.
A double-blind, placebo-controlled trial was carried out on 40 patients suffering from moderately advanced dementia. The patients were allocated randomly either pyritinol (800 mg daily) or identical placebo for 3 months. Assessments using a modified Crichton Geriatric Behavioural Rating Scale were made pre-treatment and monthly up to 3 months, and then at follow-up at 6 months. Patients on pyritinol showed significantly higher levels of improvement than did those on placebo. Laboratory tests conducted throughout remained within normal limits for both groups.
对40名中度晚期痴呆患者进行了一项双盲、安慰剂对照试验。患者被随机分配接受脑复新(每日800毫克)或相同的安慰剂,为期3个月。使用改良的克里顿老年行为评定量表在治疗前、治疗后每月直至3个月进行评估,然后在6个月时进行随访评估。服用脑复新的患者比服用安慰剂的患者改善程度明显更高。两组患者在整个试验过程中进行的实验室检查均保持在正常范围内。