Goldstein S E, Birnbom F
J Clin Psychiatry. 1979 Dec;40(12):520-4.
This study was designed to assess the effectiveness and the safety of nylidrin HCL in the geriatric patient and mild to moderate symptoms of cognitive, emotional and physical impairment. Following a 3 week placebo washout, 60 patients received either nylidrin HCL or placebo for 12 weeks. Efficacy evaluations were made utilizing the Sandoz Clinical Assessment Geriatric (SCAG) Scale, a nurse's rating of ward behavior (SCASNO), the Hamilton Psychiatric Rating Scale for Depression, and 2 of the Katz Adjustment Scales. Significant improvement in symptom severity was demonstrated in the nylidrin group as compared to the placebo group. There were no abnormalities of clinical significance in the safety measurements and few side effects were reported.
本研究旨在评估盐酸尼立替林在老年患者中对认知、情感和身体轻度至中度损害症状的有效性和安全性。在进行为期3周的安慰剂洗脱期后,60名患者接受了12周的盐酸尼立替林或安慰剂治疗。使用桑多兹老年临床评估量表(SCAG)、护士对病房行为的评分(SCASNO)、汉密尔顿抑郁量表以及卡茨适应量表中的两项进行疗效评估。与安慰剂组相比,尼立替林组症状严重程度有显著改善。安全性测量中未发现具有临床意义的异常情况,且报告的副作用较少。