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临床试验/EUCTR2017-004420-30-IE
EUCTR2017-004420-30-IE进行中(未招募)1 期

Efficacy and safety of bumetanide oral liquid formulation in children aged from 2 to less than 7 years old with Autism Spectrum Disorder. A 6-month randomised, double-blind, placebo controlled multicentre parallel group study to evaluate efficacy and safety of bumetanide 0.5mg twice a day followed by an open label active 6-month treatment period with bumetanide (0.5mg twice a day) and a 6 weeks discontinuation period after treatment stop.

Institut de Recherches Internationales Servier0 个研究点目标入组 200 人开始时间: 2019年1月11日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
200

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

入选标准

  • - Male and female patients from 2 to less than 7 years
  • - Out patients
  • - Primary diagnosis of ASD as per DSM-5 criteria
  • - Criteria met for ASD on Autism Diagnostic Observation Schedule (ADOS-2) and Autism Diagnosis Interview Revised (ADI-R)
  • - CGI (Clinical Global Impression) – Severity rating Score = 4
  • - Childhood Autism Rating Scale second edition (CARS2-ST or HF) total
  • raw score = 34
  • - Social Responsiveness Scale second edition total score (SRS-2 T-Score) = 66
  • - Absence of known monogenic syndrome (Fragile X, Rett syndrome ...)
  • - Absence of any clinically significant abnormality likely to interfere with the conduct of the study according to the judgment of the investigator
  • - Absence of electrolyte imbalance that is likely to interfere with the study conduct or evaluation
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 200
  • 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

  • - Patients not able to follow the study assessments defined by the protocol, with the exception of self-rating questionnaires which will be assessed by parent/legal representative/caregiver for those patients unable to complete them
  • - Patients having a high suicidal risk according to the investigator judgement
  • - Chronic renal dysfunction
  • - Chronic cardiac dysfunction
  • - Patient with unstable psychotherapy, behavioural, cognitive or cognitive-behavioural therapy

研究者

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