跳至主要内容
临床试验/CTRI/2025/07/090651
CTRI/2025/07/090651尚未招募2 期

A Study to compare the haemodynamic changes with and without Priming Principle with Propofol induction

Priyanka1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年8月1日最近更新:

试验速览

阶段
2 期
状态
尚未招募
发起方
入组人数
50
试验地点
1
主要终点
Reduction in induction dose of propofol and hemodynamic stability

研究概览

简要总结

Main purpose of the study is to know the required induction dose of propofol using priming principle and hemodynamic stability after induction with propofol.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • Asa Grade I and grade II Patients undergoing elective surgeries under general anaesthesia.

排除标准

  • Known allergy to propofol History of opioid abuse Pregnant and lactating women.

结局指标

主要结局

Reduction in induction dose of propofol and hemodynamic stability

时间窗: Reduction in induction dose of propofol and hemodynamic stability | Immediately after induction and At 3min,5min ,10min after induction

次要结局

  • Haemodynamic stability(Immediately after induction, at 3min,5min,10min after induction)

研究者

发起方
Priyanka
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Priyanka

Mahadevappa Rampure Medical College

研究点 (1)

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