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临床试验/NCT02383134
NCT02383134Unknown不适用

The Maximum Effective Needle-to-Nerve Distance for Anesthetic Ultrasound-Guided Supraclavicular Brachial Plexus Block

Tunisian Military Hospital0 个研究点目标入组 44 人开始时间: 2015年5月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
44
主要终点
Success of the ultrasound guided supraclavicular block at 30 minutes after injection at a specific distance of the needle tip from the outer sheeth of the nerve

研究概览

简要总结

The achievement of peripheral nerve block requires several needle passes, with each of them being at risk of causing nerve injury either by direct trauma or intraneural injection even with the use of the ultrasound.

The ultrasound guided supraclavicular brachial plexus block is known to be at risk of pneumothorax and / or nerve injury.

This study is designed to determine the maximal effective distance away from the nerve for the injection to be effective.

研究设计

研究类型
Observational
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
否

入选标准

  • •ASA physical status I-III
  • •18-85 years of age, inclusive
  • •surgery less than 3 hours

排除标准

  • •contraindications to brachial plexus block (e.g., allergy to local anesthetics, coagulopathy, malignancy or infection in the area)
  • •existing neurological deficit in the area to be blocked
  • •pregnancy
  • •history of neck surgery or radiotherapy
  • •inability to understand the informed consent and demands of the study

结局指标

主要结局

Success of the ultrasound guided supraclavicular block at 30 minutes after injection at a specific distance of the needle tip from the outer sheeth of the nerve

时间窗: 30 minutes

次要结局

  • •The onset time of sensory and motor block(the block success will be assessed for each patient every 5 min for 30 mins in the operating room beginning when the needle exits the skin)
  • The proportion of inadequate and failed blocks.(the block success will be assessed for each patient every 5 min for 30 mins in the operating room beginning when the needle exits the skin)
  • The presence of other complications such as hematoma, infection, pneumothorax.(up to 48 hours post operative.)

研究者

发起方
Tunisian Military Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr trabelsi walid

associate professor, MD

Tunisian Military Hospital

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