跳至主要内容
临床试验/NCT05691920
NCT05691920尚未招募3 期

Ultrasound Guided External Oblique Intercostal Plane Block and Pectointercostal Plane Block for Perioperative Analgesia in Coronary Artery Bypass Graft Surgery: Prospective Randomized Controlled Study

Alexandria University0 个研究点目标入组 120 人开始时间: 2023年2月1日最近更新:
适应症

试验速览

阶段
3 期
状态
尚未招募
入组人数
120
主要终点
Postoperative fentanyl requirements for 24 hours

研究概览

简要总结

Pain control after CABG is an essential step to guard against postoperative complications such as lung atelectasis. This major step can be achieved by opioids or regional blocks.

Regional blocks allow better pain control and avoid side effects of opioid based pain control

详细描述

Ultrasound guided External oblique intercostal plane block and pectointercostal plane block for perioperative analgesia in coronary artery bypass graft surgery: Prospective randomized controlled study

Introduction:

Pain control is a vital component to achieve enhanced recovery after cardiac surgery. Effective postoperative pain control will reduce the incidence of numerous postoperative complications, can facilitate early mobilization and may result in earlier recovery.

Pain control is historically achieved by the administration of opioids, which is associated with well-documented side effects, such as sedation, respiratory depression, pruritus, hallucinations and postoperative nausea and vomiting (PONV). Enhanced recovery following coronary artery bypass grafting (CABG) has gained attention even though there is limited evidence on the efficacy and effectiveness of existing analgesic techniques.

The external oblique intercostal plane and pectointercostal plane blocks are a new modality that will be used to improve pain-related outcomes after CABG surgery, and has not been extensively investigated. Therefore, we will test the hypothesis that external oblique intercostal plane and pectointercostal plane blocks can reduce cumulative opioid consumption for the patients undergoing CABG surgery when added to conventional multi-model intravenous analgesic technique.

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
Double (Participant, Investigator)

盲法说明

Double blinded

入排标准

性别
All
接受健康志愿者

入选标准

  • patients undergoing CABG surgery

排除标准

  • BMI above 40
  • allergy for drugs used
  • complicated cases
  • patient refusal
  • chronic opioid use
  • cognitive dysfunction
  • chronic kidney disease

结局指标

主要结局

Postoperative fentanyl requirements for 24 hours

时间窗: 24 hours postoperatively

Visual analogue score will be measured every 2 hours

次要结局

  • Visual analogue score(24 hours postoperatively)
  • Side effects(24 hours postoperatively)
  • Rescue analgesia(24 hours postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

相似试验