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临床试验/NCT06391541
NCT06391541Unknown不适用

Comparison of the Effects of Modified Thoracolumbar Interfacial Plan Block (mTLIP) and Intertransverse Process Block in Lumbar Disc Surgery

Zonguldak Bulent Ecevit University2 个研究点 分布在 2 个国家目标入组 90 人开始时间: 2024年4月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
90
试验地点
2
主要终点
postoperative opioid consumption

研究概览

简要总结

to compare ultrasonography (USG)-guided intertransverse process block and modified thoracolumbar interfascial plan (mTLIP) block in the treatment of postoperative pain in patients undergoing lumbar disc herniation surgery under general anesthesia.

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
Double (Participant, Outcomes Assessor)

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

  • 18-75 years old
  • ASA I-II-III risk group
  • Patients whose consent was obtained with an informed consent form
  • Patients who will undergo lumbar disc herniation surgery

排除标准

  • Patients who refused to participate in the study
  • Allergic to local anesthetics
  • Patients with coagulopathy
  • Infection at the site of intervention
  • Patients under 18 years of age
  • Patients with ASA score IV and above
  • Chronic pain disorders
  • Those with neurological or neuromuscular disease
  • Patients with psychiatric problems
  • Patients with a history of opioid use
  • Chronic use of NSAIDs
  • Those contraindicated for regional anesthesia
  • Patients with a history of opioid use
  • Chronic analgesic use

结局指标

主要结局

postoperative opioid consumption

时间窗: up to 24 hours after surgery

total amount of opioids consumed in 24 hours postoperatively

次要结局

  • incidence of nausea and vomiting(up to 24 hours after surgery)
  • Quality of Recovery-15 scale(24 hours after surgery)
  • pain scores(up to 24 hours after surgery)

研究者

发起方
Zonguldak Bulent Ecevit University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Çağdaş Baytar

Principal Investigator

Zonguldak Bulent Ecevit University

研究点 (2)

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mTLIP vs. ITP Blocks in Lumbar Disc Surgery | 临床试验