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临床试验/EUCTR2019-001677-81-NO
EUCTR2019-001677-81-NO
进行中(未招募)
1 期

Remifentanil tapering and post-adenotonsillectomy pain in children: a randomised, placebo controlled, double blind study - Paediatric Remifentanil Tapering Study

Akershus Universitetssykehus0 个研究点目标入组 60 人2019年8月13日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
Tonsillectomy and adenotonsillectomy
发起方
Akershus Universitetssykehus
入组人数
60
状态
进行中(未招募)
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
2019年8月13日
结束日期
待定
最后更新
2年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

发起方
Akershus Universitetssykehus

入排标准

入选标准

  • American Society Anaesthesiology I\-II children 1 to 10 years Weight over 10\.0 Kg
  • Undergoing day case tonsillectomy or adentonsillectomy at Akershus Universitetssykehus, Lørenskog, Norway
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 60
  • 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

  • Children who have had airway surgery previously.
  • Children who have had any type of surgery in the previous 12 monhts. Children using chronic pain medication or who have used analgesia in the 24 hours preceeding surgery.
  • Children who are known to suffer from NSAID sensitive asthma. Children with a known allergy to propofol or remifentanil.
  • Pre\-existing cardiac, renal, liver dysfunction.
  • Children or parents who are not fluent in Norwegian or English. Children in whom more than three attempts at intravenous cannulation are required or in those who request an inhalational induction or premedication.

结局指标

主要结局

未指定

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