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临床试验/NCT00150592
NCT00150592已完成2 期

A Phase II Study to Assess the Safety, Tolerability and Efficacy of SPD503 Administered to Children and Adolescents Aged 6-17 With Attention-Deficit/Hyperactivity Disorder (ADHD)

Shire0 个研究点目标入组 182 人开始时间: 2005年5月12日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
Shire
入组人数
182
主要终点
Change From Baseline in Choice Reaction Time (CRT) at 6 Weeks

研究概览

简要总结

The purpose of this study is to determine the effects of SPD503 compared to placebo on tasks of sustained attention in children and adolescents aged 6-17 diagnosed with ADHD.

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
6 Years 至 17 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Subjects with a primary diagnosis of ADHD
  • Minimum baseline visit ADHD-RS-IV score of 24 and a baseline CGI-S score =>4
  • Male or non-pregnant female subject who agrees to comply with any applicable contraceptive requirements
  • Subject weighs > 55 lbs and is not morbidly overweight

排除标准

  • Subject has a comorbid psychiatric diagnosis (except ODD) with significant symptoms such as any severe comorbid Axis II disorders or severe Axis I disorders
  • Subject has a history of seizure disorder
  • Subject has any specific cardiac condition or family history of significant cardiac condition
  • Subject is pregnant, lactating or within six month post-partum

研究组 & 干预措施

SPD503 (Guanfacine HCl)

Experimental

干预措施: SPD503 (Guanfacine HCl) (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Change From Baseline in Choice Reaction Time (CRT) at 6 Weeks

时间窗: Baseline and 6 weeks

Choice reaction time (CRT) is a computerized assessment that trains the subject in holding down a press-pad and releasing the press-pad in response to stimuli presented on the screen. The task requires the subject to react as soon as a yellow dot appears in one of five locations, and the subject must respond by lifting their hand from the press-pad. This is the reaction time (RT) and ranges from 100 to 5000 msec. Lower scores indicate better performance.

次要结局

  • Change From Baseline in Pediatric Daytime Sleepiness Scale (PDSS) Scores at 6 Weeks(Baseline and 6 weeks)
  • Change From Baseline in Digital Symbol Substitution Task/Coding Test (DSST/Coding) Scores at 6 Weeks in Age Category 8-17 Years(Baseline and 6 weeks)
  • Change From Baseline in DSST/Coding Scores at 6 Weeks in Age Category 6-7 Years(Baseline and 6 weeks)
  • Change From Baseline in Spatial Working Memory (SWM) Scores at 6 Weeks(Baseline and 6 weeks)
  • Change From Baseline in Attention Deficit Hyperactivity Disorder Rating Scale (ADHD-RS-IV) Total Score at 6 Weeks(Baseline and 6 weeks)
  • Number of Participants With Improvement in Clinical Global Impression-Improvement (CGI-I) at 6 Weeks(6 weeks)
  • Change From Baseline in Pictorial Sleepiness Scale (PSS) Scores at 6 Weeks(Baseline and 6 weeks)

研究者

发起方
Shire
申办方类型
Industry
责任方
Sponsor

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