Study of effect of intranasal ketamine on postoperative analgesia in children - A one year single blinded hospital based randomized placebo controlled clinical trial

DR APOORVA S1 个研究点分布在 1 个国家目标入组 104 人开始时间: 2023年1月8日最近更新: 2023年7月24日

试验速览

阶段: 不适用
状态: 尚未招募
发起方: DR APOORVA S
入组人数: 104
试验地点: 1
主要终点: Assessement for postoperative pain after intranasal administration of ketamine

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

KETAMINE, A NMDA antagonist has been extensively used for induction of general anaethesia . It’s use in subanaestheic doses for analagesia is being explored. Hence, this study is being undertaken to study the effect of intranasal ketamine in post operative pain relief.

研究设计

研究类型: Interventional
分配方式: Computer generated randomization
盲法: Participant Blinded

入排标准

年龄范围: 5.00 Year(s) 至 18.00 Year(s)（—）
性别: All

入选标准

•1.CHILDREN IN THE AGE GROUP 5 TO 18 YEARS UNDERGOING SURGERY UNDER GENERAL ANAESTHESIA
•CHILDREN IN ASA GRADE I TO II.

排除标准

•CHILDREN WITH
•ALLERGIC TO STUDY DRUG
•ASA GRADE III OR > III
•ABERRANT NASAL ANATOMY THAT PRECLUDES INTRANASAL MEDICATIONS.
•PATIENTS UNDERGOING ANY NASAL SURGERY.

结局指标

主要结局

Assessement for postoperative pain after intranasal administration of ketamine

时间窗: At 15, 30,45,60 min, | 2,6, 12, 24 hours post operatively using modified Childrenâ€™s Hospital of Eastern Ontario Pain Scale (CHEOPS) and Visual Analog Scale

次要结局

To determine the total amount of analgesic(Anagesia required in first 24 hours post operatively)

研究者

发起方

DR APOORVA S

申办方类型

Other [self]

研究点 (1)

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