跳至主要内容
临床试验/NL-OMON41393
NL-OMON41393
招募中
不适用

Intranasal administration of oxytocin in children with Prader-Willi Syndrome. A randomized, double-blind, placebo-controlled cross-over trial. Effects on satiety and food intake, and social behaviour.;Amendment: Six months open-label extension to the original study - Intranasal administration of oxytocin in PWS

Stichting Kind en Groei0 个研究点目标入组 28 人待定

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Prader-Willi syndrome
发起方
Stichting Kind en Groei
入组人数
28
状态
招募中
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
待定
结束日期
待定
最后更新
2年前
研究类型
Interventional

研究者

发起方
Stichting Kind en Groei

入排标准

入选标准

  • Children with Prader\-Willi syndrom, genetically confirmed diagnosis
  • Age between 6 and 14 years

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)

结局指标

主要结局

未指定

相似试验

撤回
不适用
Intranasal administration of oxytocin in children with Prader-Willi Syndrome. A randomized, open-label, cross-over trial of different treatment regimens of oxytocin administration. Effects on eating behaviour and social behaviour.
NL-OMON43050Stichting Kind en Groei44
进行中(未招募)
1 期
Intranasal administration of oxytocin in children with Prader-Willi SyndromePrader-Willi syndromeMedDRA version: 19.0Level: PTClassification code 10036476Term: Prader-Willi syndromeSystem Organ Class: 10010331 - Congenital, familial and genetic disordersTherapeutic area: Diseases [C] - Hormonal diseases [C19]
EUCTR2016-003820-22-NLDutch Growth Research Foundation
Unknown
不适用
Intranasal administration of oxytocin in PWSGenetically confirmed diagnosis of Prader-Willi syndrome
NL-OMON21542Dutch Growth Research FoundationWestzeedijk 106, 3016 AH RotterdamTel: 010-2251533info@kindengroei.nl28
进行中(未招募)
1 期
Intranasal administration of oxytocin in children and young-adults with Prader-Willi syndromePrader-Willi syndromeMedDRA version: 17.0Level: PTClassification code 10036476Term: Prader-Willi syndromeSystem Organ Class: 10010331 - Congenital, familial and genetic disordersTherapeutic area: Diseases [C] - Hormonal diseases [C19]
EUCTR2013-004134-15-NLDutch Growth Research Foundation
终止
4 期
Does intranasal oxytocin enhance emotions in dementia?Alzheimer's diseaseVascular dementiaNeurological - Alzheimer's diseaseNeurological - Dementias
ACTRN12617001531303niversity of Sydney4