跳至主要内容
临床试验/EUCTR2006-000788-27-GB
EUCTR2006-000788-27-GB进行中(未招募)1 期

International Collaborative Infantile Spasms Study (ICISS) - ICISS

Royal United Hospital Bath NHS Trust0 个研究点目标入组 410 人开始时间: 2006年3月6日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
410

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • The clinical features of Infantile Spasms confirmed by the consultant in charge or his/her nominated deputy.
  • An EEG that is hypsarrhythmic or similar, compatible with the diagnosis of Infantile Spasms.
  • Signed informed consent has been given.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • More than 72 hours has elapsed since the EEG was performed.
  • More than 72 hours has elapsed since the clinical features were confirmed.
  • Age less than two months or greater than one year and two months.
  • A diagnosis or high risk of tuberous sclerosis (known affected parent, previously diagnosed cardiac rhabdomyoma, hypomelanic macules, forehead fibrous plaque, shagreen patch, retinal phakoma or known polycystic kidneys).
  • Previous treatment for infantile spasms other than a therapeutic trial of pyridoxine to exclude pyridoxine dependent seizures. Note - previous treatment for other seizure types is not a reason for exclusion.
  • Previous treatment (within the last 28 days) with vigabatrin or hormonal treatments.
  • A contraindication to vigabatrin or hormonal treatments. A risk of a visual field defect is not considered a contraindication.
  • A lethal or potentially lethal condition, other than infantile spasms, with a risk of death before 18 months of age.
  • Doubt about the ability of the parents or guardians to know when the spasms stop.This is likely to include parents known to be intravenous drug abusers.
  • Unavailable for follow up to 18 months of age.
  • Those enrolled in a concurrent trial that is still in the active phase.
  • The language ability of the parents or guardians is such that they may not understand what is being requested of them.
  • The language ability of the parents or guardians is such that it will not be possible to undertake the Vineland assessment.

研究者

发起方
Royal United Hospital Bath NHS Trust

相似试验