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临床试验/EUCTR2014-001560-35-NL
EUCTR2014-001560-35-NL进行中(未招募)1 期

Bumetanide in Autism Medication and BIomarker study - BAMBI

Brain Center Rudolf Magnus, University Medical Center Utrecht, Department of Psychiatry, Utrecht , the Netherlands0 个研究点开始时间: 2016年1月13日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方

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

  • 1.Males or females aged =7 years to =15 years;
  • 2.Criteria met for autism on Autism Diagnostic Observation Schedule - Generic (ADOS G) and Social Responsiveness Scale (SRS) (24).
  • 3.Written informed consent.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 90
  • 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

  • 1.Total IQ < 55 (WISC) and/or inability to comply with the protocol-specified procedures for the duration of the study, including treatment, blood sampling to control diuretic effects.
  • 2.Serious, unstable illnesses including, gastroenterologic, respiratory, cardiovascular (QT interval lengthening), endocrinologic, immunologic, or hematologic disease;
  • 3.Renal or hepatic dysfunction that would interfere with excretion or metabolism of Bumetanide;
  • 4.Neurological disorders such as epilepsy, seizures and microcephaly;
  • 5.Behavioral treatment
  • 6.Treatment with psychoactive medications, including anticonvulsants, in the last 8 weeks prior to start of the study, except melatonin; no use of other psychoactive substances is allowed from 8 weeks prior to the pre-study evaluation until the endpoint measurements at the end of the washout period. If clinically feasible and desired by the patients and/or parents, then it is allowed to stop psychoactive medication to allow enrollment in the study after a 8 week washout period of their psychoactive medication.
  • 7.Treatment with NSAIDS or aminoglycosides.
  • 8.Documented history of hypersensitivity reaction to sulfonamide derivatives.

研究者

发起方
Brain Center Rudolf Magnus, University Medical Center Utrecht, Department of Psychiatry, Utrecht , the Netherlands

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