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临床试验/NCT06663449
NCT06663449尚未招募不适用

Comparison of ESP Block and STAP Plane Block in Laparoscopic Cholecystectomy Surgery

Kocaeli University1 个研究点 分布在 1 个国家目标入组 68 人开始时间: 2024年12月15日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
68
试验地点
1
主要终点
NRS Scores

研究概览

简要总结

In order to effectively manage postoperative analgesia in patients planned to undergo elective laparoscopic cholecystectomy, patients will be divided into 2 (two) groups and informed consent forms will be obtained after the necessary information is provided so that both groups can be included in the study. In the group planned to undergo erector spinae plane block, erector spinae plane block will be performed after monitoring and sedation in the operating room block unit before being taken to the surgical table preoperatively and postoperative PCA analgesia will be applied. In patients who will undergo subcostal transversus abdominis plane block, subcostal tap block will be performed after monitoring and sedation in the operating room block unit before being taken to the surgical table preoperatively and postoperative PCA analgesia will be applied. The patients' perioperative pain will be monitored with NOL (nociception level) monitor. Remifentanil dose will be adjusted to keep the NOL level between 10 and 25. After the patients are followed up for 24 hours postoperatively, their additional analgesia needs and amounts during this process will be compared. In this way, it is aimed to show that the analgesic method can be used effectively in the follow-up of pain management by comparing the Erector Spina Plane block and the Subcostal Transversus Abdominis Plane block as an effective analgesic application in laparoscopic cholecystectomy operations.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients who will undergo laparoscopic cholecystectomy:
  • 18-75 years old
  • ASA I-II-III patients

排除标准

  • Use of anticoagulant drugs
  • Known allergy to drugs to be used
  • Infection in the area where the block will be performed
  • Patient's reluctance

结局指标

主要结局

NRS Scores

时间窗: 1 hours after surgery(T1), 3 hours after surgery (T2), 6 hours after surgery (T3), 12 hours after surgery (T4) and 24 hours after surgery(T5)

NRS scores of the patients after the surgery (0=no pain, 10=worst pain imaginable)

Morphine consumption

时间窗: 1 hours after surgery(T1), 3 hours after surgery (T2), 6 hours after surgery (T3), 12 hours after surgery (T4) and 24 hours after surgery(T5)

Amount of morphine consumption (mg)

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

Sevim Cesur

principal investigator

Kocaeli University

研究点 (1)

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