跳至主要内容
临床试验/CTRI/2024/02/063181
CTRI/2024/02/063181已完成不适用

Comparision of quantitative use of sevoflurane with high initial concentration Vs incremental induction technique in children at a tertiary care centre

Sri Ramachandra Institute of Higher Education and Research1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年5月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
70
试验地点
1
主要终点
Quantity of inhalation agent requirement

研究概览

简要总结

This is a Randomised single blinded study comparing the requirement of the inhalation agent Sevoflurane for inhalational induction of anesthesia in children. One group gets induced with a fixed 8% Sevoflurane whereas the other group receives incremental doses as 2% for 10 seconds  followed by 4% and 6% for 10 seconds then increased to 8%. The drug requirement, time to I’ve cannulation and hemadynamic parameters are compared between the 2 groups

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
1.00 Year(s) 至 12.00 Year(s)(—)
性别
All

入选标准

  • •Children between the age group of 1 to 12 posted for elective surgeries.

排除标准

  • •Known history of allergies to inhalation agents Any contraindications to inhalation induction Emergency surgery.

结局指标

主要结局

Quantity of inhalation agent requirement

时间窗: Quantity of inhalation agent consumption measured at the end of induction of anesthesia

次要结局

  • Time taken for ease of IV cannulation(Hemadynamics parameters)

研究者

申办方类型
Private medical college

研究点 (1)

Loading locations...

相似试验

Comparision of quantitative use of sevoflurane with... | 临床试验