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临床试验/NCT04224844
NCT04224844暂停不适用

Ultrasound-Guided Spinae Plane Block for Perioperative Pain Control in Carotid Endarterectomy.

Antalya Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 34 人开始时间: 2020年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
暂停
发起方
入组人数
34
试验地点
1
主要终点
24 hours tramadol consumption

研究概览

简要总结

The purpose of this study is to test the hypothesis that erector spinae plane block will decrease intraoperative local anesthetic and postoperative analgesic consumption in patients undergoing carotid endarterectomy.

详细描述

Patients who decided to participate in the study will be randomized into 2 groups: Erector Spinae Plane Block Group (Group E) and Control Group (Group C). Intraoperative local anesthetic consumption, postoperative tramadol consumption, intraoperative and pain scores, hemodynamic parameters and patient satisfaction will be recorded.

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
Single (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

  • Patients undergoing carotid endarterectomy
  • American Society of Anesthesiologists class 2 to 3
  • Ability to consent

排除标准

  • inability to communicate
  • not understand the aim and objectives of the study
  • not provide informed written consent
  • contraindications for the block (local infection, coagulation disorders)
  • hypersensitivity to the local anesthetics
  • refusal of regional anesthesia

结局指标

主要结局

24 hours tramadol consumption

时间窗: 24 hours

Total tramadol consumption in milligrams at 24 hrs will be scored.

6 hours tramadol consumption

时间窗: 6 hours

Total tramadol consumption in milligrams at 6 hrs will be scored.

12 hours tramadol consumption

时间窗: 12 hours

Total tramadol consumption in milligrams at 12 hrs will be scored.

Assesment of postoperative analgesia

时间窗: 12 hours

Post operative pain scores will be assessed using a numerical rating scala (NRS) (from 0=no pain, to10= worst pain imaginable) at 12 hours.

次要结局

  • Amount of use of intraoperative local anesthetic.(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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