Ulnar Nerve Block for Procedural Anesthesia - Wrist Versus Palm
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
- 是
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)
