Lewis D M, Bond H R, Curry S H
Psychopharmacology (Berl). 1983;80(3):259-62. doi: 10.1007/BF00436165.
In a study with both open and double-blind phases, a therapeutic response to sulpiride was first established in 18 chronic schizophrenic inpatients. Following this, two dosage regiments, a morning only dose, and the same daily total dose in two equal fractions at 8 a.m. and 4 p.m., were compared using a balanced design, crossover, placebo controlled study. Clinical effects were evaluated by means of the Brief Psychiatric Rating Scale (BPRS). There was a significant reduction in the mean BPRS score in all phases of the study. There was no significant difference between the mean BPRS scores resulting from the two dosage regimens. The study indicated that the two dosage regimens were equally efficacious.
在一项包含开放期和双盲期的研究中,首先在18名慢性精神分裂症住院患者中确定了舒必利的治疗反应。在此之后,采用平衡设计、交叉、安慰剂对照研究,比较了两种给药方案,即仅早晨给药一次,以及每日总剂量相同但分两次在上午8点和下午4点等量给药。通过简明精神病评定量表(BPRS)评估临床效果。在研究的所有阶段,BPRS平均得分均显著降低。两种给药方案产生的BPRS平均得分之间没有显著差异。该研究表明两种给药方案疗效相当。