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临床试验/NCT04895072
NCT04895072已完成不适用

Effect of Injection Rate on the Block Sensory Level in the Erector Spine Plane Block

Antalya Training and Research Hospital2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2021年5月17日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Block sensory level

研究概览

简要总结

To evaluate the effect of injection rate on the block sensory level in the ESP block.

详细描述

Many women experience severe acute postoperative pain after breast cancer surgery. Regional techniques are frequently used as a part of multimodal analgesia in breast surgery. Ultrasound-guided erector spinae plane (ESP) block is a preferred method to reduce the postoperative opioid requirement for postoperative pain management. In this study, we aimed to evaluate the effect of injection rate on the block sensory level in the ESP block.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • aged between eighteen and sixty-five
  • ASA I-III
  • undergo elective breast cancer surgery

排除标准

  • under 18 years of age or over 65 years of age
  • ASA IV and above
  • declined to give written informed consent
  • contraindications of peripheral blocks or local anesthetic infiltration
  • history of allergy against local anesthetics
  • chronic pain history
  • history of hepatic, neuromuscular, cardiac and/or renal failure
  • infection at the injection site

结局指标

主要结局

Block sensory level

时间窗: 12 hours

Number (average) of dermatomes with sensory block with pinprick and cold methods after the ESP block

次要结局

  • Postoperative tramadol consumption(24 hours)
  • Assesment of postoperative analgesia(24 hours)

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 (2)

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