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临床试验/NCT04669639
NCT04669639已完成不适用

A Comparison of Erector Spinae Plane Block to Suprascapular Nerve Block for Analgesia in Shoulder Surgery

Zagazig University1 个研究点 分布在 1 个国家目标入组 96 人开始时间: 2020年12月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
96
试验地点
1
主要终点
Intraoperative analgesia

研究概览

简要总结

A comparison between Erector Spinae Plane block and Suprascapular nerve block in providing analgesia for shoulder surgery

详细描述

Suprascapular nerve block is considered a phrenic nerve sparing approach that recently introduced as alternative for interscalene brachial plexus nerve block in shoulder surgery. However, some researchers reported that Suprascapular nerve block alone results in an ineffective analgesia. Erector Spinae Plane block is supposed to be able in providing adequate analgesia in shoulder surgery

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
盲法
Double (Care Provider, Outcomes Assessor)

盲法说明

The care provider and outcome assessor will be unaware of the study design

入排标准

年龄范围
21 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •ASA I and II,
  • •Age above 21 years and below 60 years in both sexes,
  • •Cooperative patients,
  • •Patients with a BMI (body mass index) not exceeding 35.

排除标准

  • •patients with cardiovascular or respiratory compromise,
  • •Patient refusal,
  • •Coagulopathy,
  • •Local tissue infection,
  • •Allergy to local anesthesia,
  • •prior to cervical or thoracic spine surgery.

研究组 & 干预措施

The block group (a)

Experimental

Patients were randomized in a 1:1 :1ratio, group (a) will receive SSN. The nerve blocks The procedure will be performed after induction of anaesthesia and endotracheal intubation.

干预措施: Block procedures for shoulder surgery analgesia (Other)

The block group (b)

Experimental

Patients were randomized in a 1:1:1 ratio. group (b) will receive the Erector spinae plane block. The procedure will be performed after induction of anesthesia and endotracheal intubation.

干预措施: Block procedures for shoulder surgery analgesia (Other)

control group

Placebo Comparator

Patients were randomized in a 1:1:1 ratio. this group will receive general anesthesia (GA) only

干预措施: Block procedures for shoulder surgery analgesia (Other)

结局指标

主要结局

Intraoperative analgesia

时间窗: The intraoperative patients' hemodynamics every 30 min were collected and analyzed till the end of surgery . Also the total dose of opioids consumed intraoperatively will be recorded. Postoperative consumed opioid for 24 hours also will calculated

Recording of the patients' hemodynamics (heart rate and non-invasive blood pressure) and total dose of opioids consumption intraoperatively and postoperatively.

次要结局

未报告次要终点

研究者

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

Naglaa Fathy Abdelhaleem Abdelhaleem

Lecturer, Anesthesia and Surgical Intensive Care department, Faculty of Medicine

Zagazig University

研究点 (1)

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