Ultrasound Guided Erector Spinae Plane Efficacy of Erector Spinae Plane Block for Analgesia in Breast Surgery
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 42
- 试验地点
- 1
- 主要终点
- Total opioid consumption
研究概览
简要总结
Patients were randomized into two groups, ESP and control. Single-shot ultrasound (US)-guided ESP block with 20 ml 0.25% bupivacaine at the T4 vertebral level was performed preoperatively to all patients in the ESP group. The control group received no intervention. Patients in both groups were provided with intravenous patient-controlled analgesia device containing morphine for postoperative analgesia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Patients who scheduled for bilateral reduction mammoplasty
- •ASA Class I-II
排除标准
- •Coagulopaty
研究组 & 干预措施
erector spinae plane block group
Single-shot ultrasound (US)-guided ESP block with 20 ml 0.25% bupivacaine at the T4 vertebral level
干预措施: Erector Spinae Plane Block (Procedure)
control group
morphine pca to patient
干预措施: Standart therapy (Procedure)
结局指标
主要结局
Total opioid consumption
时间窗: Postoperative total opioid consumption in miligrams will be recorded at hour 24
Patients in both groups will receive opioid in postoperative period. Total opioid consumption in miligrams will be compared
次要结局
- Intraoperative opioid consumption(At the end of the operation)
研究者
Gözde Gamze Uzun
Consultant Anesthesiologist
Kocaeli University