A comparative study of haemodynamic responses of propofol induction between BIS guided dose and sleep dose

Sentila Shangne1 个研究点分布在 1 个国家目标入组 92 人开始时间: 2021年12月6日最近更新: 2021年3月6日

试验速览

阶段: 4 期
状态: 尚未招募
发起方
入组人数: 92
试验地点: 1
主要终点: To compare sleep guided dose of propofol with BIS guided dose on haemodynamic response

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

A randomised controlled trial will be conducted in my institution to compare the haemodynamic responses of propofol using the sleep dose of Propofol and BIS guided dose of Propofol and their comparison

研究设计

研究类型: Interventional
分配方式: Coin toss, Lottery, toss of dice, shuffling cards etc
盲法: Not Applicable

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 1&2 Elective surgeries under general anaesthesia Patients with a signed informed written consent form.

排除标准

•Patient refusal History of cardiac diseases like dilated cardiomyopathy,CCF, Arrhythmias etc History of uncontrolled hypertension and hypotension Patients with hepatic or renal dysfunction, pregnancy or any serious medical conditions that would interfere with cardiovascular response Patients with history of allergy to any GA drugs Cases lasting less than 30mins.

结局指标

主要结局

To compare sleep guided dose of propofol with BIS guided dose on haemodynamic response

时间窗: Baseline,15minutes intraoperative and 15minutes postoperatively

次要结局

To Assess sedation scale(Postoperative Period upto 48 hrs)

研究者

发起方

Sentila Shangne

申办方类型

Other [self]

研究点 (1)

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