Cohn J B, Wilcox C
J Clin Psychiatry. 1985 Mar;46(3 Pt 2):26-31.
The efficacy and safety of fluoxetine were compared with those of imipramine and of placebo in a 6-week randomized double-blind parallel study of patients with major depressive illness. Mean values for all efficacy measurements were improved over baseline with fluoxetine and imipramine treatment (p less than .001). More fluoxetine patients completed the study than did imipramine or placebo patients. Predominant adverse experiences reported by imipramine patients were dry mouth and dizziness/lightheadedness. Predominant adverse experiences reported by fluoxetine patients were drowsiness/sedation and excessive sweating. In a subsequent 48-week open-label study, the predominant adverse experience in the fluoxetine group was excessive sweating and in the imipramine group was still dry mouth. In this study, fluoxetine relieved the symptoms of major depressive illness effectively and significantly better than placebo and was better tolerated than imipramine.
在一项针对重度抑郁症患者的为期6周的随机双盲平行研究中,比较了氟西汀与丙咪嗪及安慰剂的疗效和安全性。使用氟西汀和丙咪嗪治疗后,所有疗效测量的平均值均较基线有所改善(p<0.001)。完成研究的氟西汀患者比丙咪嗪或安慰剂患者更多。丙咪嗪患者报告的主要不良反应是口干和头晕/头重脚轻。氟西汀患者报告的主要不良反应是嗜睡/镇静和多汗。在随后一项为期48周的开放标签研究中,氟西汀组的主要不良反应是多汗,而丙咪嗪组仍然是口干。在本研究中,氟西汀能有效缓解重度抑郁症的症状,且显著优于安慰剂,耐受性也优于丙咪嗪。