跳至主要内容
临床试验/NCT06437743
NCT06437743尚未招募不适用

Monitoring Nociception Using NoL Index and Its Implications in Reducing Opioid-Related Complications in Laparoscopic Abdominal Surgery

Investigation Group Anesthesia, Resuscitation, And Perioperative Medicine of Aragon0 个研究点目标入组 282 人开始时间: 2024年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
282
主要终点
Reduction in Postoperative Opioid-Related Complications

研究概览

简要总结

This study aims to determine if optimal intraoperative nociception monitoring using the NoL index can reduce postoperative complications related to opioid use in laparoscopic abdominal surgery. The hypothesis is that guided nociception monitoring decreases opioid-related complications and improves postoperative outcomes.

详细描述

The study is a prospective, observational cohort study conducted across multiple centers. It aims to evaluate the impact of intraoperative nociception monitoring on postoperative opioid-related complications. The study will involve two groups of patients undergoing laparoscopic abdominal surgery: one group with visible NoL monitoring and another with non-visible NoL monitoring.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Age ≥ 18 years
  • Scheduled for laparoscopic abdominal surgery
  • Undergoing balanced general anesthesia
  • ASA physical status I-III
  • Signed informed consent

排除标准

  • Refusal to participate
  • Communication barriers
  • Multimodal, opioid-free, or regional epidural anesthesia
  • ASA IV or V
  • Pregnant or breastfeeding women
  • Open or emergency abdominal surgery
  • Post-surgery transfer to ICU or Recovery Unit

结局指标

主要结局

Reduction in Postoperative Opioid-Related Complications

时间窗: From the end of surgery up to 48 hours postoperatively

The primary outcome measure will evaluate the incidence of postoperative opioid-related complications in patients undergoing laparoscopic abdominal surgery. Complications include nausea, vomiting, respiratory depression, and opioid-induced hyperalgesia. The study aims to determine if the use of the NoL monitor to guide intraoperative analgesia reduces these complications compared to standard hemodynamic monitoring.

次要结局

  • Postoperative Pain Scores(At 1, 6, 12, 24, and 48 hours postoperatively)
  • Length of Hospital Stay(From admission to discharge, up to 7 days postoperatively)
  • Intraoperative Opioid Consumption(During the surgical procedure)

研究者

发起方
Investigation Group Anesthesia, Resuscitation, And Perioperative Medicine of Aragon
申办方类型
Network
责任方
Sponsor

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