NCT05537831尚未招募不适用
Ultrasound Guided vs Landmark-based Hematoma Block in Distal Forearm Fractures
State University of New York - Upstate Medical University0 个研究点目标入组 96 人开始时间: 2022年9月1日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 96
- 主要终点
- Pain relief from landmark versus ultrasound guided hematoma block
研究概览
简要总结
This is a randomized control trial comparing the efficacy of ultrasound (US) guided vs landmark-guided hematoma blocks on distal forearm fractures.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 7 Years 至 —（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients greater than and equal to seven years of age
- •Patients with traumatic acute distal radius/ulnar fractures with displacement that require reduction and immobilization with splinting
- •Patients that receive distal radius hematoma blocks, including those who require additional pain control adjuncts if pain control is not adequate
排除标准
- •Prisoners
- •Pregnant women
- •Patients with altered mental status/have impaired decision-making capacity.
- •Patients with allergies to amide anesthetics
结局指标
主要结局
Pain relief from landmark versus ultrasound guided hematoma block
时间窗: Change in pain score from before the hematoma block to immediately after the reduction/splinting of the forearm fracture
Pain will be measured using a ten point Likert scale with zero designated as no pain and ten being the worst pain the patient can imagine. The higher score the worse the outcome.
次要结局
未报告次要终点
研究者
Paul Klawitter
Associate Profressor
State University of New York - Upstate Medical University
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