Comparison of the Analgesic Efficacy of Erector Spinae Plane Block in Lumbar Microdiscectomy Surgeries
Comparison of the Analgesic Efficacy of Lumbar Erector Spinae Plane Block and Sacral Erector Spinae Plane Block in Lumbar Microdiscectomy Surgeries
研究概览
地位
详细说明
Postoperative pain is commonly observed in patients undergoing lumbar microdiscectomy surgery.
To manage this pain, the lumbar erector spinae plane (ESP) block is frequently administered as part of a multimodal analgesia regimen, particularly with the aim of reducing opioid consumption in these patients.
Recent publications have demonstrated the analgesic efficacy of the sacral erector spinae plane block in lumbar microdiscectomy surgeries.
In this study, the postoperative analgesic effectiveness of the lumbar ESP block-performed two vertebral levels above the surgical site-will be compared with that of the sacral ESP block-performed two vertebral levels below the surgical site.
It is anticipated that this approach will provide effective analgesia while avoiding the use of opioids.
研究类型
注册 (实际的)
联系人和位置
学习地点
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Istanbul、土耳其（türkiye）
- Gaziosmanpasa Research and Training Hospital
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
取样方法
研究人群
描述
Inclusion Criteria:
ASA I, ASA II, and ASA III patients scheduled for single-level lumbar microdiscectomy at the L4-L5 or L5-S1 level.
Exclusion Criteria:
Pregnant patients
Patients who do not consent to the erector spinae plane block
Patients requiring mechanical ventilatory support
Patients with a history of substance abuse
Patients with a known allergy to the medications to be used
Patients with bleeding diathesis
Patients with infection at the planned block site
Patients undergoing surgical intervention at two or more spinal levels
Patients with communication difficulties or intellectual disabilities
Patients with neuropsychiatric disorders
Patients with chronic pain
Patients with an expected surgical duration of 180 minutes or more
Patients with a prior history of lumbar microdiscectomy
学习计划
研究是如何设计的？
设计细节
队列和干预
团体/队列 |
|---|
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lumbar ESP
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sacral ESP
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研究衡量的是什么？
主要结果指标
结果测量 |
大体时间 |
|---|---|
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total tramadol consumption
大体时间：first 24 hours after the surgery
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first 24 hours after the surgery
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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patients' visual analog scale
大体时间：first 24 hours after the surgery
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To compare postoperative Visual Analog Scale (VAS) pain scores at 2, 4, 8, 12, and 24 hours.
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first 24 hours after the surgery
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To compare analgesic consumption during the postoperative time intervals of 0-2, 2-4, 4-8, 8-12, and 12-24 hours.
大体时间：first 24 hours after the surgery
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postoperative 0-2, 2-4, 4-8, 8-12, and 12-24 hours.
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first 24 hours after the surgery
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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