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临床试验/CTRI/2021/11/037896
CTRI/2021/11/037896尚未招募不适用

Comparison between intranasal DEXMEDITOMIDINE versus intranasal KETAMINE as premedication for intravenous access in children-Randamised control study

DrAnilin Joeyself1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2021年11月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
To compare the efficacy of intranasal DEXMEDITOMIDINE to facilitate the intravenous access in children

研究概览

简要总结

It is a randomised,prospective,comparative,double blinded observational study wherein intranasal DEXMEDITOMIDINE and Ketamine are compared to facilitate the intravenous access in children.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

入排标准

年龄范围
3.00 Month(s) 至 5.00 Year(s)(—)
性别
All

入选标准

  • 1.Age between 3 months to 5 years 2.ASA grade 1 &2&3 3.Weight of the patient being in normal range for that age and sex.

排除标准

  • Patients with ASA physical status IV or more.
  • Patients with any neurological and psychiatric disorders.
  • History of allergy to any of the drugs being used under study.
  • Unwilling patients.

结局指标

主要结局

To compare the efficacy of intranasal DEXMEDITOMIDINE to facilitate the intravenous access in children

时间窗: Sedation score: | Grade1-10minute-separation from mother | Grade2- 10-20minutes-Awake but separated easily | Grade3-20-30minutes-Difficult to separate easily

次要结局

  • Efficacy of intranasal KETAMINE to facilitate the intravenous access in children(Sedation score:)

研究者

发起方
DrAnilin Joeyself
申办方类型
Other []

研究点 (1)

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