跳至主要内容
临床试验/CTRI/2024/09/073328
CTRI/2024/09/073328尚未招募不适用

A prospective observational study on correlation of induction dose of propofol according to different body weight metrics.

TRIHMS1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年9月10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
40
试验地点
1
主要终点
To find out the best propofol induction dose among different body weight metrics.

研究概览

简要总结

A prospective observational study on the correlation of induction dose of propofol according to different body weight metrics going to be done on 40 patients in patients undergoing elective surgery.

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 55.00 Year(s)(—)
性别
All

入选标准

  • ASA-PS I & II ROUTINE SURGERY CASE UNDER GENERAL ANAESTHESIA.

排除标准

  • UNCONTROLLED HYPERTENSION ISCHEMIC HEART DISEASE RENAL OR HEPATIC DYSFUNCTION SUSPECTED SUBSTANCE ABUSE.

结局指标

主要结局

To find out the best propofol induction dose among different body weight metrics.

时间窗: during induction

次要结局

  • Any serious adverse event.(During induction period.)

研究者

发起方
TRIHMS
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Dusu Lalin

Tomo Riba Institute of Health and Medical Sciences.

研究点 (1)

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