Spinal for Laparoscopic Cholecystectomy
试验速览
- 阶段
- 不适用
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Patient satisfaction (over a scale from 1 to 4)
研究概览
简要总结
In this study, the investigators will study spinal anesthesia for laparoscopic cholecystectomy in comparison to general anesthesia (GA) regarding patient satisfaction as a primary variable, intraoperative complications, postoperative analgesic requirements, postoperative nausea and vomiting, patient hospital stay (secondary variables).
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
- None
入排标准
- 年龄范围
- 18 Years 至 45 Years（Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •patients scheduled for laparoscopic cholecystectomy
排除标准
- •coagulopathy
- •Patient refusal
- •previous spine surgery
- •Obesity BMI more than 30
研究组 & 干预措施
General anesthesia group
General anesthesia group: Standard anesthetic technique will be applied.Anesthesia will be induced by propofol 1% (1-2 mg/kg), Fentanyl 1-2 mic/kg, and Atracurium 0.5 mg/kg then according to train of four response. Then maintained using Sevoflurane based anesthesia aiming to maintain Bispectral index 40-60..
干预措施: General anesthesia (Drug)
Spinal anesthesia group
While in sitting position; intrathecal injection using 25 G spinal needle using 3 mls of Bupivacaine 0.5% with 20 mic Fentanyl, at L 2-3 level the patient head will be lowered till sensory blockade of T6 obtained at least.
干预措施: Bupivacaine with Fentanyl (Spinal Anesthesia) (Drug)
结局指标
主要结局
Patient satisfaction (over a scale from 1 to 4)
时间窗: 24 hours
Postoperative analgesic consumption (mg morphine)
时间窗: 24 hours
次要结局
未报告次要终点