Schachter S C, Vazquez B, Fisher R S, Laxer K D, Montouris G D, Combs-Cantrell D T, Faught E, Willmore L J, Morris G L, Ojemann L, Bennett D, Mesenbrink P, D'Souza J, Kramer L
Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, MA 02215, USA.
Neurology. 1999 Mar 10;52(4):732-7. doi: 10.1212/wnl.52.4.732.
To evaluate the efficacy and safety of oxcarbazepine in a placebo-control trial.
A multicenter, double-blind, randomized, placebo-control, two-arm parallel group, monotherapy design was used to compare oxcarbazepine administered 1,200 mg twice daily to placebo in hospitalized patients with refractory partial seizures, including simple and complex partial seizures and partial seizures evolving to secondarily generalized seizures. Patients exited the trial after completing the 10-day double-blind treatment phase or after experiencing four partial seizures, two new-onset secondarily generalized seizures, serial seizures, or status epilepticus, whichever came first.
Analysis of the primary efficacy variable--time to meeting one of the exit criteria--showed a statistically significant effect in favor of oxcarbazepine (p = 0.0001). The secondary efficacy variables--percentage of patients who met one of the exit criteria (p = 0.0001) and total partial seizure frequency per 9 days during the double-blind treatment (p = 0.0001)--were also statistically significant in favor of oxcarbazepine.
These results demonstrate that oxcarbazepine given as monotherapy is effective and safe for the treatment of partial seizures in this paradigm.
在一项安慰剂对照试验中评估奥卡西平的疗效和安全性。
采用多中心、双盲、随机、安慰剂对照、双臂平行组单药治疗设计,将每日两次服用1200毫克奥卡西平的住院难治性部分性癫痫患者(包括简单部分性发作、复杂部分性发作以及演变为继发性全身性发作的部分性发作)与安慰剂进行比较。患者在完成10天双盲治疗阶段后,或经历4次部分性发作、2次新发性继发性全身性发作、连续发作或癫痫持续状态(以先出现者为准)后退出试验。
对主要疗效变量——达到退出标准之一的时间——的分析显示,奥卡西平具有统计学上的显著疗效(p = 0.0001)。次要疗效变量——达到退出标准之一的患者百分比(p = 0.0001)以及双盲治疗期间每9天的部分性发作总频率(p = 0.0001)——在统计学上也显著有利于奥卡西平。
这些结果表明,在该模式下,奥卡西平单药治疗对部分性癫痫有效且安全。