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临床试验/NCT04634721
NCT04634721已完成不适用

Transversus Abdominis Plan Block Applied in Laparoscopic Cholecystectomies Effective By Which Method: Ultrasound or Laparoscopic?

Ankara City Hospital Bilkent1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2020年11月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
Mean postoperative static and dynamic numeric rating scale (NRS) at 24 hours

研究概览

简要总结

Abdominal wall blocks are frequently used as part of multimodal analgesia for pain control after abdominal surgery. There are studies using the Transversus Abdominis Plane Block for postoperative pain control in laparoscopic cholecystectomies.

In this study, the investigators aimed to compare the advantages of these two methods by applying the Transversus Abdominis Plan Block for postoperative pain control after laparoscopic cholecystectomy with the help of postoperative USG and laparoscopy during surgery.In this study, the investigators aimed to compare the advantages of these two methods by applying the Transversus Abdominis Plan Block for postoperative pain control after laparoscopic cholecystectomy with the help of postoperative USG and LAPAROSCOPY during surgery.

详细描述

A total of 60 patients aged 18-65, ASA 1-2-3, who will undergo elective laparoscopic cholecystectomy in our hospital, will be included in the study. Patients will be randomly divided into 3 groups with ultrasound (USG) guided (GROUP 1: USG) , Laparoscopic application (GROUP 2: LAP) and GROUP 3 :No-TAP blok Each group consists of 20 evil people. Written consent will be obtained by explaining the procedure to be performed before the operation to the patients. The Transversus Abdominis Plan Block will be applied to the patients by a blind anesthesiologist according to their group. The block to be made by the anesthesiologist who will apply the block procedure will be given in a closed envelope.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Other
盲法
Single (Participant)

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

  • ASA I,II,III
  • Patients 18-65
  • laparoscopic cholecystectomy

排除标准

  • ASA III higher
  • history of pain relief medication dependence
  • history of substance abuse
  • end stage chronic kidney disease
  • advanced liver disease
  • history of chronic pain -history of taking opioids or neuropathic agents regularly prior to surgery-
  • BMI of 50 or over
  • skin infections at the site of TAP block injection or port sites.

研究组 & 干预措施

Laparoscopic TAP block

Active Comparator

Laparoscopic assisted TAP block will be done by surgeon intra-operatively

干预措施: bupivacaine (Drug)

Ultrasaund TAP block

Active Comparator

injecting bupivacaine in transversus abdominis plane to block the somatic nerves

干预措施: bupivacaine (Drug)

结局指标

主要结局

Mean postoperative static and dynamic numeric rating scale (NRS) at 24 hours

时间窗: 24 hours

o compare the mean NRS at 0hr, 1hr, 2 hrs. 6 hrs. 12 hrs. and 24hrs. post-operatively between three groups Numeric rating scale for pain,(0=no pain, 1-3= mild pain, 4-6 moderate pain, 7-10 severe pain.)

次要结局

  • Post operative nausea or vomiting(24 hours)

研究者

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

Mehmet sahap

Principal Investigator

Ankara City Hospital Bilkent

研究点 (1)

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