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临床试验/CTRI/2024/02/062548
CTRI/2024/02/062548尚未招募不适用

A comparison of 10% lignocaine spray versus eutectic mixture of 2.5% lidocaine and 2.5% prilocaine (EMLA) to attenuate pain of peripheral venous cannulation in adults: A prospective randomised single-blind placebo-controlled trial

未提供1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2024年2月21日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
90
试验地点
1
主要终点
To Assess and compare degree of severity of pain during IV cannulation using the

研究概览

简要总结

Baseline vitals will be taken after group allocation, and one group will get 10% lignocaine spray while the other group will receive emla cream. The VAS score will be assessed in both the study groups for measuring pain immediately after cannulation and 10 mins later. Additionally hemodynamic parameters and grading of ease of cannulation will also be noted The study aims to compare the efficacy of 10% lignocaine spray and  EMLA cream in reducing pain associated with peripheral venous cannulation

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • American society of anesthesiology (ASA I to IV).

排除标准

  • Refusal to participate Difficult iv cannulations Any burns, ulceration, erythema and infected skin · Any allergic to amide local anaesthetic History of deep vein thrombosis or any other vascular disorder · History of cardiac disease or migraine headachesPregnant or lactating females.

结局指标

主要结局

To Assess and compare degree of severity of pain during IV cannulation using the

时间窗: Immediately after cannulation and 10 mins later

visual analogue scale (VAS) pain score

时间窗: Immediately after cannulation and 10 mins later

次要结局

  • To observe any change in hemodynamics – BP, HR, SPO2 after topical application(of study drugs.)

研究者

发起方
未提供
责任方
Principal Investigator
主要研究者

Mona K

Mahatma Gandhi Medical college and Research Institute

研究点 (1)

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