临床试验/CTRI/2025/02/080233

CTRI/2025/02/080233尚未招募1 期

Effectiveness of lignocaine pretreatment vs lignocaine mixed with propofol in preventing pain due to propofol injection : a randomised control study

Dr SUMANTH S1 个研究点分布在 1 个国家目标入组 140 人开始时间: 2025年2月28日最近更新: 2025年2月5日

试验速览

阶段: 1 期
状态: 尚未招募
发起方
入组人数: 140
试验地点: 1
主要终点: compare the frequency of pain reported by the patient during injection using numerical pain rating scale

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

Comparison between effectiveness of lignocaine pretreatment and lignocaine mixed with propofol in preventing pain due to propofol injection as propofol on injection causes pain and there are various methods to relieve this pain . so we want to compare to such methods to decrease the pain due to propofol injection in an actual daily routine practice after premedicating the patients while the previous studies are done without premedication

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

•patients willing to give informed consent and belong to ASA 1 and ASA 2.

排除标准

•patient not willing to give informed written consent patient with risk factors for difficult airway patient with known pulmonary and cardiovascular diseases known allergy to local anesthetic,propofol obese patients patients who are mentally unstable,visually impaired patient with difficult intravenous access or with less than 20g cannula in situ.

结局指标

主要结局

compare the frequency of pain reported by the patient during injection using numerical pain rating scale

时间窗: Pain score during injection of propofol

次要结局

compare the frequency of pain reported by the patient just before shifting out the patient from recovery using numerical pain rating scale(pain just before shifting out the patient from recovery)

研究者

发起方

Dr SUMANTH S

申办方类型

Other [self]

责任方

Principal Investigator

主要研究者

Sumanth S

ESIC PGIMSR

研究点 (1)

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