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临床试验/NCT07179731
NCT07179731尚未招募不适用

Comparison of the Effects of External Oblique Intercostal Plane Block, Subcostal Transverse Abdominis Plane Block, and Their Combination in the Management of Postoperative Pain in Laparoscopic Cholecystectomy Surgery

Istanbul Medeniyet University0 个研究点目标入组 105 人开始时间: 2025年9月23日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
105
主要终点
Postoperative Analgesic Consumption

研究概览

简要总结

This study aims to compare the efficacy of Subcostal Transversus Abdominis Plan Block, External Oblique Intercostal Plan Block and the combination of these two blocks, which are used in anesthesiology practice for postoperative pain in laparoscopy cholecystectomy surgery.

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
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients scheduled for laparoscopic cholecystectomy surgery
  • •Patients aged between 18 to 80 years
  • •Having an anesthesiology risk assessment of ASA I, II, or III

排除标准

  • •Patients who do not give written and oral consent
  • •Patients with coagulopathy
  • •History of allergic reaction or intoxication by local anesthetics
  • •Severe organ failure
  • •Mental retardation or illiteracy
  • •Presence of infection on the injection site
  • •Pregnancy
  • •Patients whom the procedure is extended to open cholecystectomy

研究组 & 干预措施

Group 1: subcostal transversus abdominis plane block

Active Comparator

This group will receive 30 ml 0.25% of bupivacaine for the subcostal transversus abdominis plane block prior to surgery.

干预措施: subcostal transversus abdominis plane block (Procedure)

Group 2: external oblique intercostal plane block

Active Comparator

This group will receive 30 ml 0.25% of bupivacaine for the external oblique intercostal plane block prior to surgery.

干预措施: External Oblique Intercostal Plane Block (Procedure)

Group 3: subcostal transversus abdominis and external oblique intercostal plane block combination

Active Comparator

This group will receive 15 ml 0.25% of bupivacaine for the external oblique intercostal plane block, in combination with 15 ml 0.25% of bupivacaine for the subcostal transversus abdominis plane block prior to surgery.

干预措施: external oblique intercostal plane block and subcostal transversus abdominis plane block combination (Procedure)

结局指标

主要结局

Postoperative Analgesic Consumption

时间窗: 24 hours postoperatively

The opioid consumption via patient controlled analgesia (PCA) in 24 hours postoperatively

次要结局

  • Postoperative Pain Scores(up to 24 hours after surgery)

研究者

发起方
Istanbul Medeniyet University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Faruk Komez

MD

Istanbul Medeniyet University

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