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临床试验/NCT06717672
NCT06717672已完成3 期

Efficacy of Lidocaine in Decreasing Perioperative Analgesic Opioids Requirement After Ambulatory Surgery

Liaquat National Hospital & Medical College1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2023年11月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
80
试验地点
1
主要终点
Peri-operative pain

研究概览

简要总结

  1. *Reduced opioid consumption
  2. *Decreased pain scores
  3. *Fewer opioid-related side effects
  4. *Improved patient satisfaction

详细描述

Studies have shown that lidocaine can reduce opioid consumption by 20-50% in the perioperative period.

Studies have shown that lidocaine can reduce opioid consumption by 20-50% in the perioperative period.

By reducing opioid consumption, lidocaine can also decrease the incidence of opioid-related side effects, such as nausea, vomiting, and respiratory depression.

Lidocaine's analgesic effects can improve patient satisfaction and reduce anxiety related to pain

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • ASA 1 and 2
  • patient age between 18 and 65 years
  • Patient undergoing ambulatory surgeries

排除标准

  • Pregnant women
  • Allergic to Lidocaine Patient who had fever and treated with antibiotic and steroid in last month

研究组 & 干预措施

Intervention group

Active Comparator

intervention group recieve inj lidocaine

干预措施: Lidocaine 2% without vessel constrictor (Drug)

Control group

Placebo Comparator

control group receive Normal saline

干预措施: Normal Saline (Drug)

结局指标

主要结局

Peri-operative pain

时间窗: at 2 hours, 4 hours, 6 hours

Visual Analog pain scale to rate pain scale comprises 0 to 10 score 0 minimum to 10 Maximum

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Hanesh Tanwani

Principal Investigator

Liaquat National Hospital & Medical College

研究点 (1)

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