NL-OMON42266撤回4 期
Pediatric Analgesia via the Intra-Nasal route. An observational multicenter prospective cohort study of atomized intranasal fentanyl in pediatric trauma patients in the emergency department - PAI
Rode Kruis Ziekenhuis0 个研究点目标入组 128 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 撤回
- 发起方
- 入组人数
- 128
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 2 至 17（—）
入选标准
- •Pediatric traumapatients >2yrs in the Emergency Department
- •Pain due to fractures, dislocations, wounds or burns
- •Receiving intranasal fentanyl
排除标准
- •Children younger than 2 yrs
- •No administration of intranasale fentanyl because of nasal obstruction, nose bleed or allergy for fentanyl
- •Legal guardian not able to sign informed consent
研究者
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 disordersEUCTR2016-003820-22-NLDutch Growth Research Foundation
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 studyPrader-Willi syndrome10083624NL-OMON41393Stichting Kind en Groei28
Unknown
不适用
Intranasal administration of oxytocin in PWSGenetically confirmed diagnosis of Prader-Willi syndromeNL-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 disordersEUCTR2013-004134-15-NLDutch Growth Research Foundation