Erector Spinae Regional Anesthesia for Pain Control in the Emergency Department
试验速览
- 阶段
- 早期 1 期
- 状态
- 已完成
- 入组人数
- 15
- 试验地点
- 3
- 主要终点
- Pain Scale Rating
研究概览
简要总结
Interventional study to use erector spinae plane block (ESPB) on diagnoses of posterior or lateral rib fractures, vertebral fractures, pancreatitis, pancreatic cancer, renal colic, and back pain for multimodal pain therapy to determine its assistance with pain relief as well as the patient's use of opiates after block completion
详细描述
Patients with the listed diagnoses will be offered and then consented for an ESPB under ultrasound guidance. They will rate their pain before and 30 minutes after the procedure using the ordinal categorical data on a numeric pain scale. Total patient opiate use will be gathered up to 8 hours after block completion.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Posterior/lateral rib or vertebral fractures
- •Pancreatitis or pancreatic cancer
- •Renal colic
- •Back pain
排除标准
- •Unstable vitals
- •Infection or open wound over insertion site
- •Prior allergic reaction to local anesthetic
- •Pregnant females
- •Patients <18 years old
- •Altered mentation
研究组 & 干预措施
Erector Spinae Plane Block (ESP) administration
Patients with the listed diagnoses will be offered and then consented for an ESPB under ultrasound guidance.
干预措施: Bupivacaine Injection (Drug)
结局指标
主要结局
Pain Scale Rating
时间窗: Baseline to study procedure end (approximately 30 minutes)
Change in pain scale rating assessed by the participants on a scale from 0-10 with 0 indicating no pain and 10 indicating the most severe pain.
次要结局
未报告次要终点