临床试验/CTRI/2024/07/070229

CTRI/2024/07/070229尚未招募Unknown

To compare the effect of two methods of propofol delivery on pain on injection of propofol A randomized study

Lewlyna Eireeka Ivan1 个研究点分布在 1 个国家目标入组 330 人开始时间: 2024年7月12日最近更新: 2024年7月1日

试验速览

阶段: Unknown
状态: 尚未招募
发起方
入组人数: 330
试验地点: 1
主要终点: NRS score at 5 sec after administration of 0.2mg/kg of propofol injection

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

Propofol is the most widely used intravenous anaesthetic agent for induction, sedation and maintenance of anesthesia. The most common side effect of propofol is pain on injection which patients can remember even postoperatively. Hence, our aim is to find the most efficacious way to reduce pain on propofol injection.

研究设计

研究类型: Interventional
分配方式: Randomized
盲法: Participant and Investigator Blinded

入排标准

年龄范围: 18.00 Year(s) 至 60.00 Year(s)（—）
性别: All

入选标准

•ASA I-III scheduled under GA with Propofol as the agent of intravenous induction.

排除标准

•Patient refusal to participate
•Patients with known allergy to egg
•Patients scheduled for emergency surgeries, patients with severe valvular heart disease.

结局指标

主要结局

NRS score at 5 sec after administration of 0.2mg/kg of propofol injection

时间窗: NRS score at 5 sec after administration of 0.2mg/kg of propofol injection

次要结局

Blood pressure and heart rate at baseline and after propofol injection, any redness or inflammation at the iv cannulation site(At 5 seconds)

研究者

发起方

Lewlyna Eireeka Ivan

申办方类型

Other [Self funding ]

责任方

Principal Investigator

主要研究者

Lewlyna Eireeka Ivan

Sri Ramachandra Institute of Higher Education and Research

研究点 (1)

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