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临床试验/NCT05913167
NCT05913167招募中不适用

Comparison of Erector Spina and Transversus Abdominus Plan Blocks

Kocaeli University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年8月15日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
2
主要终点
Postoperative morphine consumption

研究概览

简要总结

Nephrectomy pain was higher. erector spina plan block and transversus abdominis plan block had shown to be effective in abdominal surgeries. This study aimed to compare these two bloc analgesic efficacy in laparoscopic nephrectomy patients. The primary aim is postoperative morphine consumption.

详细描述

Patients ASA 18-65 who will undergo laparoscopic nephrectomy are included in this prospective randomized clinical trial. Patients will be divided into two groups; erector spina and transversus abdominis plane block. Anesthesia will. induced with propofol, fentanyl, and rocuronium will be administered for muscle relaxation. Bispectral index monitoring will be used for monitorisation of the depth of anesthesia. Remifentanil was used during the whole procedure. the amount of consumption will be recorded. Patient-controlled device will be used with morphine. The postoperative morphine consumption will also be recorded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Diagnostic
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Participants will not know which block was administered outcome assessors will not know which block was administered

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-65 age
  • patients undergoing laparoscopic nephrectomy

排除标准

  • <18- >65 < age
  • patients undergoing open nephrectomy

结局指标

主要结局

Postoperative morphine consumption

时间窗: 24 hour postoperatively

morphine patient controlled analgesia was applied to the patients

次要结局

  • postoperative analgesia numeric rating scales(postoperative 24 hours)
  • Peroperative remifentanil consumptions(peroperatively)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Zehra Ipek ARSLAN

Professor

Kocaeli University

研究点 (2)

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