跳至主要内容
临床试验/NCT00595751
NCT00595751已完成不适用

Best Estimate Diagnosis Used to Evaluate EEG in Association With ADHD in a Multi-Site, Clinical Sample of Children and Adolescents

Lexicor Medical Technology, LLC10 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2007年12月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
300
试验地点
10
主要终点
'Best Estimate Diagnosis' of ADHD applied in the intended population in settings with the intended users

研究概览

简要总结

The study will evaluate the effectiveness of a standardized EEG method with the intended clinical users in the intended clinical settings with the intended population (patients who would typically receive a clinician's evaluation for ADHD). Multiple sites will be examined to provide a sample of patients across numerous communities with different demographics. The goal is to evaluate if the predictive accuracy of EEG will not be inferior to that of a widely-used and extensively validated ADHD scale in the prediction of ADHD in the intended use population as evaluated by Best Estimate Diagnosis.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Subject willing to voluntarily participate in a research study that includes EEG collection and analysis.
  • Family/patient seeking comprehensive clinical evaluation for attention and/or behavior concerns.
  • Male or female at least 6 years of age and who will not be over 17.99 years of age upon admission to study.
  • Willing to stop any and all current psychiatric medications prior to or by entry into study.
  • Subject and parent (or legal representative) of an educational level and degree of understanding sufficient to communicate suitably with the investigator, rater and study coordinator.

排除标准

  • Previous diagnosis of mental retardation. IQ < 70 by previous records.
  • History of seizure disorder or of EEG abnormalities. On anticonvulsants for seizure control.
  • Metal plate or metal device in the head.
  • Suicide ideation or gesture and/or homicidal ideation or gesture.
  • Concomitant medications during participation in a research study. No prescription or nonprescription medications with psychoactive properties that may affect EEG (such as over-the-counter dietary supplements, pseudoephedrine, or phenylpropanolamine). No antipsychotics, no psychostimulants, no antidepressants. Washout of at least one week or longer depending on the medication and clinician's judgment. Medication used for medical reasons must be cleared by research staff with consideration of known effects on EEG.
  • Known serious medical problems (cardiovascular, hematological, liver, seizure disorder, renal, or chronic respiratory problems).

结局指标

主要结局

'Best Estimate Diagnosis' of ADHD applied in the intended population in settings with the intended users

时间窗: At prensentation to clinic with attention or behavior problems

次要结局

未报告次要终点

研究者

发起方
Lexicor Medical Technology, LLC
申办方类型
Industry

研究点 (10)

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