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临床试验/NCT00643136
NCT00643136已完成3 期

Pregabalin BID Add-on Trial: a Randomized, Double-Blind, Placebo-Controlled Parallel-Group Single-Center Sleep EEG Study in Patients With Partial Seizures and Sleep Disturbance Part B: a Randomized, Double-Blind, Placebo-Controlled Parallel-Group Study of Pregabalin Add-on Treatment

Pfizer1 个研究点 分布在 1 个国家目标入组 17 人开始时间: 2002年11月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Pfizer
入组人数
17
试验地点
1
主要终点
Change from baseline in polysomnographic (PSG) sleep efficiency in the efficacy evaluable population

研究概览

简要总结

The purpose of this study is to determine the effects of pregabalin on sleep problems in patients with seizures.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Partial epileptic seizures
  • Not taking more than 1 background antiepileptic drug at study entry
  • Disturbed sleep

排除标准

  • More than 1 secondarily generalized tonic/clonic seizure per week on average over the previous 3 months
  • Medical, psychological, or social conditions that could interfere with normal sleep

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

Pregabalin

Experimental

干预措施: Pregabalin (Drug)

结局指标

主要结局

Change from baseline in polysomnographic (PSG) sleep efficiency in the efficacy evaluable population

时间窗: Endpoint

次要结局

  • Change from baseline in total sleep time(Endpoint)
  • Change from baseline in sleep onset latency(Endpoint)
  • Change from baseline in wake after sleep onset(Endpoint)
  • Change from baseline in percent sleep spent in stages 3 and 4(Endpoint)
  • Change from baseline in percent sleep spent in REM stage(Endpoint)
  • Change from baseline in night sleep quality based on Groningen Sleep Questionnaire (GSQ)(Endpoint)
  • Change from baseline in 4-week sleep quality (Medical Outcomes Study [MOS] Sleep Scale)(Endpoint)
  • Adverse events and laboratory value changes(Endpoint)

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (1)

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