跳至主要内容
临床试验/NCT05764616
NCT05764616已完成不适用

Ultrasound Guided Parasternal Block Combined With Rectus Sheath Block for Cardiac Surgery Under Sternotomy: A Randomized Controlled Trial

Campus Bio-Medico University1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2023年3月21日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
58
试验地点
1
主要终点
Static Pain Score

研究概览

简要总结

The aim of this randomized controlled trial is to examine the effect of ultrasound guided bilateral Parasternal Nerve Block combined with rectus sheath block on preoperative analgesia, opioid consumption and respiratory function in patients undergoing cardiac surgery via sternotomy. Half of participants will receive General Anesthesia combined with bilateral parasternal block and rectus sheath block while the other half receive General Anesthesia combined with bilateral parasternal block and infiltration of drainage exits sites with local anesthetic (without performing rectus sheath block)

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
None

入排标准

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

入选标准

  • Patients undergoing elective cardiac surgery under median sternotomy
  • Age >= 18 years
  • American Society of Anesthesiologists (ASA) Status I-IV
  • Approval and sign of the informed consent

排除标准

  • Allergy to local anesthetics
  • Puncture site infection
  • Lack of signing of informed consent
  • Age <18 years
  • Emergency surgery
  • ASA > IV
  • preoperative acute respiratory failure

结局指标

主要结局

Static Pain Score

时间窗: 24 hours

A numerical rating scale (NRS) from 0 (no pain) to 10 (worst imaginable pain) will be used to evaluate pain at rest during 24 hours after surgery

Dynamic Pain Score

时间窗: 24 hours

A numerical rating scale (NRS) from 0 (no pain) to 10 (worst imaginable pain) during movement will be used to evaluate pain at rest during 24 hours after surgery

次要结局

  • Time of Extubation(48 hours)
  • Intensive Care Unit (ICU) Discharge Time(120 hours)
  • Hospitalization Length of Stay(30 days)
  • Incidence of adverse events(24 hours)
  • Morphine Consumption(24 hours)
  • Respiratory performance at incentive spirometry(48 hours)
  • Intraoperative Fentanyl Consumption(4 hours)

研究者

发起方
Campus Bio-Medico University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Giuseppe Pascarella

Principal Investigator

Campus Bio-Medico University

研究点 (1)

Loading locations...

相似试验