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临床试验/EUCTR2013-004134-15-NL
EUCTR2013-004134-15-NL进行中(未招募)1 期

Intranasal administration of oxytocin in children and young adults with Prader-Willi Syndrome. A randomized, double-blind, placebo-controlled trial. Effects on satiety and food intake, and social behaviour. - Intranasal administration of oxytocin in PWS

Dutch Growth Research Foundation0 个研究点开始时间: 2014年3月20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

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

  • In order to be eligible to participate in this study, a subject must meet all of the following criteria:
  • - Genetically confirmed diagnosis of Prader-Willi syndrome
  • - Age between 3 and 25 years
  • For fMRI: age > 6 years.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 20
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 10
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Severe psychiatric problems
  • - Non cooperative behaviour
  • - Allergic reactions or hypersensitivity for oxytocin
  • - Serious illness
  • - Cardiac abnormalities
  • - Extremely low dietary intake of less than minimal required intake according to WHO
  • - Medication to reduce weight (fat)

研究者

发起方
Dutch Growth Research Foundation

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