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临床试验/NCT03744689
NCT03744689已完成不适用

The Effect Of Erector Spinae Plane Block On Postoperative Pain Management In Lumbar Disc Hernia Repair Operation

Kocaeli University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年10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
Morphine consumption

研究概览

简要总结

Pain management after lomber disc hernia repair surgery is a challenging issue for anesthetists. Erector Spinae plane block is a novel analgesic technique which could be used for this purpose. Primary aim of this double blinded randomized controlled study is to compare the analgesic efficacy of this new block technique with control group in this group of patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

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

  • Age 18-65 years
  • Undergoing elective lomber disc hernia

排除标准

  • ASA III - IV
  • infection of the skin at the site of needle puncture area
  • patients with known allergies to any of the study drugs
  • coagulopathy

研究组 & 干预措施

Erector Spinae Plane Block

Active Comparator

Erector Spinae Plane Block Group

Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks

干预措施: Erector Spinae Plane block (Procedure)

Erector Spinae Plane Block

Active Comparator

Erector Spinae Plane Block Group

Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks

干预措施: Bupivacaine Hydrochloride (Drug)

Erector Spinae Plane Block

Active Comparator

Erector Spinae Plane Block Group

Block Drug: 0,25% bupivacaine hydrochloride (20ml) will be used for blocks

干预措施: PCA (Device)

Control Group

Sham Comparator

Sham block will be done with serum physiologic.

干预措施: Sham block (Procedure)

Control Group

Sham Comparator

Sham block will be done with serum physiologic.

干预措施: PCA (Device)

结局指标

主要结局

Morphine consumption

时间窗: postoperative first 24 hour

morphine consumptions will be recorded

次要结局

  • Numeric rating scale(postoperative first 24 hour)

研究者

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

Dilek İçli

Associate professor

Kocaeli University

研究点 (1)

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