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临床试验/NCT00827658
NCT00827658终止不适用

Ulnar Nerve Block for Procedural Anesthesia - Wrist Versus Palm

Hamilton Health Sciences Corporation1 个研究点 分布在 1 个国家目标入组 127 人开始时间: 2008年2月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
127
试验地点
1
主要终点
Primary outcome is efficacy of sensory anesthesia and analgesia

研究概览

简要总结

Ulnar nerve blockade is necessary for sensory anesthesia and analgesia in the hand during minor procedures. The course of the ulnar nerve in the forearm, wrist, and hand is predictable and has low variability. However even with known anatomic location and landmarks, ulnar nerve blocks at the wrist frequently are inadequate for procedural anesthesia. The antebrachial fascia at the wrist acts as a barrier to local infiltration. Since the fascia can not be visualized or palpated, it is commonly not penetrated, resulting in an inadequate block. Furthermore at the level of the wrist the ulnar artery lies in close proximity to the nerve and there is potential for arterial puncture while attempting injection for volar wrist block. The palmar ulnar nerve block is an injection distal to the hook of the hamate in the thenar eminence which avoids the ulnar artery and antebrachial fascia. This block has been used successfully for many years in clinical practice but has not been assessed or compared in a research study. The purpose of this study is to assess the validity of using a palmar ulnar nerve block for procedures in the hand as compared to the standard volar wrist ulnar nerve block.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
Single (Investigator)

入排标准

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

入选标准

  • any individual who can give informed consent and is scheduled for elective hand procedures by the PI necessitating an Ulnar nerve block of the hand.

排除标准

  • patients unable to give informed consent
  • patients with previous or ongoing ulnar nerve deficits or neuropathy
  • patients undergoing Guyon's canal decompression
  • patients who can not comprehend or cooperate with assessment testing
  • patients with abnormal two point discrimination (> 6 mm at the test location) prior to the nerve block

结局指标

主要结局

Primary outcome is efficacy of sensory anesthesia and analgesia

时间窗: 15-45 minutes

次要结局

  • Secondary outcome is patient perceived discomfort with block(15-45 Minutes)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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