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临床试验/CTRI/2018/02/011666
CTRI/2018/02/011666已完成2 期

Efficacy of Ultrasound Guided Superficial Cervical Plexus Block for control of shoulder tip pain during Laprascopic Surgery under Spinal Anaesthesia – A Randomised Comparative Trial

Anaesthesia Department1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年12月6日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
intra operative opiod requirement

研究概览

简要总结

This study is a randomised comparative trial, investigating the efficacy of performing ultrasound guided superficial cervical plexus block to control the shoulder tip pain, without affecting the diaphragam function, thereby improving patient comfort during laparoscopic surgery under regional anaesthesia.  The primary outcome measure includes comparing the consumption of opioid analgesic during the surgery, between the two groups, which was found to be significantly less in the study group compared to the control group.  The secondary outcome measures include the incidence of conversion to general anaesthesia in which the difference was insignificant, the assessment of diaphragmatic function using ultrasound after performance of the superficial cervical plexus block which was used to correlate the occurrence and intensity of referred shoulder pain during peritoneal insufflation and the patients were found to tolerate the procedure well and there were no complications reported.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Outcome Assessor Blinded

入排标准

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

入选标准

  • ASA physical status I and II
  • Gynaecological Laparascopic surgeries under 2hours.

排除标准

  • Contraindication for spinal anaesthesia
  • Infection in the skin of the neck
  • Height less than 145cms.

结局指标

主要结局

intra operative opiod requirement

时间窗: 2 hours

次要结局

  • Diaphragmatic function Assessment by Lloyd’s method(30 minutes)
  • Patient satisfaction
  • Conversion to GA

研究者

发起方
Anaesthesia Department
申办方类型
Private medical college

研究点 (1)

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