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临床试验/NCT04706780
NCT04706780终止不适用

Hemi-diaphragmatic Paresis After Ultrasound-guided Erector Spinae Plane Block in Carotid Endarterectomy

Antalya Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2021年1月20日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
7
试验地点
1
主要终点
incidence of hemi-diaphragmatic paresis

研究概览

简要总结

To assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane (ESP) block

详细描述

The ultrasound (USG) guided ESP block was first defined in 2016. With the administration of local anesthesia between the transverse process of the vertebra and the erector spinae muscle, it is stated that the effect mechanism of ESP is that spread blocks the ventral and dorsal rami to the paravertebral area. The aim of the study is to assess the incidence of hemi-diaphragmatic paresis following ultrasound-guided erector spinae plane block.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18 - 85 years
  • American Society of Anesthesiology (ASA) I-III
  • elective carotid endarterectomy

排除标准

  • patient's refusal
  • under 18 years of age or over 65 years of age
  • ASA IV and above
  • known allergy to local anaesthetic drugs
  • the block cannot be applied due to bleeding disorders or localized skin infection at the injection site
  • history of neurological and/or neuromucular disease
  • history of severe bronchopulmonary disease
  • a moderate to severe decrease in preoperative pulmonary function, or abnormality in preoperative chest radiography data (pleural effusion, pneumothorax, or hemidiaphragm elevation)
  • emergency surgery

结局指标

主要结局

incidence of hemi-diaphragmatic paresis

时间窗: 30 minutes

Diaphragmatic excursion was measured using M-mode ultrasound during normal breathing, deep breathing and with the sniff manoeuvre.

次要结局

  • opioid consumption(1 hour)
  • Postoperative Numeric Rating Scale (NRS) score(24 hours)
  • postoperative analgesia consumption(24 hours)
  • intraoperative local anesthetic consumption(1 hour)

研究者

发起方
Antalya Training and Research Hospital
申办方类型
Other Gov
责任方
Sponsor

研究点 (1)

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