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首页> 外文期刊>Journal of child neurology >Pregabalin as Adjunctive Treatment for Focal Onset Seizures in Pediatric Patients: A Randomized Controlled Trial
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Pregabalin as Adjunctive Treatment for Focal Onset Seizures in Pediatric Patients: A Randomized Controlled Trial

机译:Praetabalin作为儿科患者局灶性发病癫痫发作的辅助治疗:随机对照试验

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Efficacy and safety of pregabalin as adjunctive treatment for children (aged 4-16 years) with partial-onset seizures, hereafter termed focal onset seizures for this study, was evaluated. This double-blind, randomized, placebo-controlled, international study had 3 phases: 8-week baseline, 12-week double-blind treatment (2-week dose escalation; 10-week fixed dose), and 1-week taper. Selection criteria included experiencing focal onset seizures and receiving a stable regimen of 1 to 3 antiepileptic drugs. Study treatments were pregabalin 2.5 mg/kg/d, 10 mg/kg/d, or placebo; doses were increased to 3.5 or 14 mg/kg/d for subjects weighing <30 kg. The key endpoints were change in log_(e)(28-day seizure rate), achieving a ≥50% seizure responder rate, safety, and tolerability during double-blind treatment. Subjects (n = 295; mean age 10.2 years, 55% male, 69% white) were randomized to pregabalin 2.5 mg/kg/d (n = 104), 10 mg/kg/d (n = 97), or placebo (n = 94). A statistically significant reduction in log_(e)(28-day seizure rate) was demonstrated with pregabalin 10 mg/kg/d (a 19.9% improvement over placebo; P = .0185). Seizure frequency was numerically improved (statistically nonsignificant) with pregabalin 2.5 mg/kg/d ( P = .2577). Responder rate significantly favored pregabalin 10 mg/kg/d (40.6%, P = .0068) compared with placebo (22.6%) and was numerically improved with pregabalin 2.5 mg/kg/d (29.1%, P = .2600). Common adverse events (≥10% of any group) in 10 mg/kg/d, 2.5 mg/kg/d, and placebo groups, respectively, included somnolence (25.8%, 17.3%, 13.8%), increased weight (13.4%, 3.8%, 4.3%), and increased appetite (10.3%, 6.7%, 4.3%). Pregabalin 10 mg/kg/d demonstrated efficacy in seizure frequency reduction in children with focal onset seizures compared with placebo, and both pregabalin doses were generally safe and well tolerated. www.clinicialtrials.gov identifier NCT01389596; EudraCT #2010-020852-79.
机译:评估了Praetabalin作为儿童的辅助治疗(4-16岁)的辅助治疗,以后评估了本研究的局灶性发作癫痫发作。这种双盲,随机,安慰剂控制的国际研究有3个阶段:8周基线,12周双盲治疗(2周剂量升级; 10周固定剂量)和1周锥度。选择标准包括体验焦点发作癫痫发作并接受1至3种抗癫痫药物的稳定方案。研究治疗是普瑞巴林2.5mg / kg / d,10mg / kg / d或安慰剂;对于称重<30kg的受试者,剂量增加到3.5或14mg / kg / d。关键终点是LOG_(e)(28天癫痫发作率)的变化,在双盲处理过程中达到≥50%的癫痫发作率,安全性和可耐受性。受试者(n = 295;平均10.2岁,55%雄性,69%白色)被随机转移到Prabalin 2.5mg / kg / d(n = 104),10mg / kg / d(n = 97),或安慰剂( n = 94)。普瑞巴林10mg / kg / d证明了Log_(e)(28天癫痫发作率)的统计学显着减少(安慰剂的提高19.9%; P = .0185)。癫痫发作频率在数值上改善(统计学上无显着性)与Prababalin 2.5mg / kg / d(p = .2577)。与安慰剂(22.6%)相比,响应者速率显着青睐10mg / kg / d(40.6%,p = .0068),用Pragabalin 2.5mg / kg / d数值改善(29.1%,p = .2600)。常见不良事件(≥10%的任何组)分别在10mg / kg / d,2.5mg / kg / d和安慰剂组中,包括嗜睡(25.8%,17.3%,13.8%),重量增加(13.4%) 3.8%,4.3%),食欲增加(10.3%,6.7%,4.3%)。与安慰剂相比,普瑞巴林10mg / kg / d证明了患有局灶性发作癫痫发作的儿童的疗效,并且Pragabalin剂量通常是安全和耐受性的。 www.clinicialtrials.gov标识符NCT01389596; eudract#2010-020852-79。

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