Hjorther A, Browne E, Jakobsen K, Viskum P, Gyntelberg F
Acta Neurol Scand. 1987 Apr;75(4):271-6. doi: 10.1111/j.1600-0404.1987.tb07932.x.
In a 12-week double-blind study, oxiracetam (CGP 21690 E), a new nootropic drug, at a dose of 2.4 mg per day, was compared to placebo in the treatment of 106 middle-aged patients suffering from mild to moderate organic brain syndrome due to prolonged exposure to organic solvents. At the beginning of the study and after 12 weeks treatment, the patients underwent a battery of neuropsychological tests to determine their mental and memory functioning. A symptom questionnaire consisting of 21 items was rated pre-treatment, and improvement or worsening of any of the symptoms recorded monthly. At the end of the study a global evaluation was performed by the patients themselves, their relatives, the psychologist and the doctor. The code was not broken until the final writing of this paper. No statistically significant differences were observed between the treatment groups in any of the above-mentioned evaluations; neither were any differences in the neuropsychological tests performance observed. Thus, oxiracetam seems to have no effect in the treatment of organic brain syndrome.
在一项为期12周的双盲研究中,将一种新型益智药奥拉西坦(CGP 21690 E)以每日2.4毫克的剂量与安慰剂进行比较,用于治疗106名因长期接触有机溶剂而患有轻至中度器质性脑综合征的中年患者。在研究开始时和治疗12周后,患者接受了一系列神经心理学测试,以确定他们的心理和记忆功能。一份由21项内容组成的症状问卷在治疗前进行评分,每月记录任何症状的改善或恶化情况。在研究结束时,由患者本人、其亲属、心理学家和医生进行总体评估。直到本文最终撰写时才解开密码。在上述任何评估中,治疗组之间均未观察到统计学上的显著差异;在神经心理学测试表现方面也未观察到任何差异。因此,奥拉西坦似乎对器质性脑综合征的治疗没有效果。