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临床试验/NCT06424938
NCT06424938已完成不适用

The Effect of Epidural Analgesia and Erector Spinae Plane Block on Intraoperative and Early Postoperative Outcomes in Open Gynecological Oncological Surgeries: a Prospective Randomized Study

Duygu Akyol1 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2024年7月1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
71
试验地点
1
主要终点
postoperative numerical rating scale

研究概览

简要总结

The aim of this study is to compare the effectiveness of epidural block or erector spinae plane block applied for postoperative analgesia in gynecological cancer surgeries.

The main question(s) it aims to answer are:

[Is erector spinae plane block as effective as epidural block in postoperative analgesia?] The study was designed as a prospective randomized study. Researchers evaluated the effects of epidural block or erector spinae plane block applied for postoperative analgesia on pain scores, postoperative opioid use, and mobilization in patients undergoing gynecological cancer surgery.

详细描述

Our study was designed as a prospective randomized study. The investigators evaluated the analgesia methods used in patients undergoing surgery for gynecologic cancer between May 2024 and December 2024. The investigators evaluated the effect of epidural block or erector spina plan block on postoperative analgesia, opioid use and mobilization.

Group 1: Epidural block group Group 2: Group with erector spina plan block

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
Single (Participant)

入排标准

年龄范围
30 Years 至 70 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients who will undergo open abdominal surgery
  • Patients with ASAII-III
  • Those between the ages of 30-70
  • Patients who are fully oriented and able to cooperate

排除标准

  • Patients with ASAIV-V
  • Presence of active infection in the area where the block will be applied
  • Patients younger than 30 years old
  • Patients with BMI > 40
  • Patients who are allergic to bupivacaine
  • Chronic analgesic use

结局指标

主要结局

postoperative numerical rating scale

时间窗: postoperatvely 24 hours

The primary purpose of this study is to compare NRS values at 0, 6, 12 and 24 hours in the first 24 hours postoperatively. Numeric rating scale was used to assess postoperative pain For example, 0-10 where 0 is no pain and 10 is the worst pain imaginable.

次要结局

  • Intraoperative amount of remifentanyl(intraoperative process)

研究者

发起方
Duygu Akyol
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Duygu Akyol

M.D

Bakirkoy Dr. Sadi Konuk Research and Training Hospital

研究点 (1)

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