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临床试验/NCT00301236
NCT00301236已完成3 期

A 5-Week Treatment, Multi-Center, Double-Blind, Randomized, Placebo-Controlled, Parallel-Group, Fixed-Dose Study of the Efficacy, Tolerability and Safety of Dexmethylphenidate HCl Extended-Release Capsules Administered Once Daily in Pediatric Children With Attention-Deficit/Hyperactivity Disorder

Novartis26 个研究点 分布在 1 个国家目标入组 252 人开始时间: 2006年2月1日最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Novartis
入组人数
252
试验地点
26
主要终点
Assessment of the symptoms by the patient's teacher after 5 weeks of treatment.

研究概览

简要总结

The purpose of this study is to determine which dosages of dexmethylphenidate HCl extended-release capsules may represent effective treatment for ADHD in children 6-12 years of age.

详细描述

The purpose of this study is to determine which dosages of dexmethylphenidate HCl extended-release capsules may represent effective treatment for ADHD in children 6-12 years of age.

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

入排标准

年龄范围
6 Years 至 12 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Children 6 - 12 with a diagnosis of ADHD of any type , Same teacher who is willing to complete the assessment during the school term

排除标准

  • Previous cardiac problems of the patient or the parents or current cardiac findings of the patient; Relevant medical condition other than ADHD; ADHD medication within a specified timeperiod prior to study start; Pregnancy or nursing; Positive drug screen
  • Other protocol-defined inclusion/exclusion criteria may apply

结局指标

主要结局

Assessment of the symptoms by the patient's teacher after 5 weeks of treatment.

次要结局

  • Assessment of the symptoms by the patient's parent after five weeks of treatment.
  • Change in severity of the illness assessed by the physician after 5 weeks of treatment
  • Improvement of the illness assessed by the physician after 5 weeks of treatment
  • Safety and tolerability of 5 week's treatment with dexmethylphenidate HCl extended-release capsules in children with Attention-Deficit/Hyperactivity Disorder by assessing the frequency of adverse findings

研究者

发起方
Novartis
申办方类型
Industry

研究点 (26)

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