NCT05247021Unknown4 期
Bilateral Ultrasound Guided Erector Spinae Plane Block for Postoperative Pain Management in Lumbar Spine Surgery ( a Controlled Study Trial)
适应症
试验速览
- 阶段
- 4 期
- 入组人数
- 44
- 试验地点
- 2
- 主要终点
- the postoperative 24 hours morphine consumption
研究概览
简要总结
Aim of this study was to assess the efficacy of erector spinae plane block (ESB) for postoperative pain management in lumbar spine surgery.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 60 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients American Society of Anesthesiologists physical status (ASA) I and II.
- •Both sexes.
- •Age between 20 to 60 years old.
- •Scheduled for lumbar spine surgeries.
排除标准
- •Patients who received long acting opioids preoperatively.
- •Patients with bleeding disorders and coagulopathy.
- •Infection at the injection site.
- •Allergy to local anesthetics.
- •Patients with significant cognitive dysfunction.
- •Patients with diabetic neuropathy.
- •Patients with uncontrolled hypertension or diabetes.
- •Patients with advanced cardiac, respiratory, hepatic or renal disease.
- •Patients with viral hepatitis or HIV.
结局指标
主要结局
the postoperative 24 hours morphine consumption
时间窗: 24 hours postoperative
the analgesic effect of erector spine block will be assessed postoperative by numeric rating scale (NRS), if NRS is more than 3 the patient will receive a rescue dose of 5 milligrams of morphine
次要结局
- Mean Blood pressure in mmHg(24 hours postoperative)
- First time of mobilization to a chair(24 hours postoperative)
- Patient satisfaction(24 hours postoperative)
- Heart rate(24 hours postoperative)
研究者
研究点 (2)
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