Ultrasound guided bilateral erector spinae plane block for lumbar spine surgery: a prospective randomized controlled double blinded study
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 74
- 试验地点
- 1
- 主要终点
- 24-hour postoperative pain scores using Numeric Rating Scare (NRS 0 - 10)
研究概览
简要总结
This single-center, prospective, randomized, double-blinded study will be conducted at Manipal Hospital Whitefield, Bangalore. Seventy four American Society of Anesthesiologists (ASA) physical status I Iland III patients aged between 30 and 70 years undergoing lumbar spine surgery under general anaesthesia will be recruited for the study. A written informed consent will be obtained from all patients enrolled in the study. Eligible patients will be randomized into two groups: 37 patients in the Erector spinae plane (ESP) block group and 37 patients in the non-ESP block group.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 30.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •American Society of Anaesthesiologists physical status 1.
排除标准
- •Patients who are allergic to local anaesthetics.
结局指标
主要结局
24-hour postoperative pain scores using Numeric Rating Scare (NRS 0 - 10)
时间窗: Baseline (0 hour in the postoperative period); 2 hours; 4 hours; 8 hours; 12 hours, 24 hours in the postoperative period
次要结局
- To compare the number of rescue analgesics needed between patients receiving and not receiving Erector spinae plane block for elective lumbar spine surgery under general anaesthesia.(24 hours after surgery)
- To compare the patients pain control satisfaction between patients receiving and not receiving Erector spinae plane block for elective lumbar spine surgery under general anaesthesia.(24 hours after surgery)
研究者
Shivananda
Department of Anaesthesiology, Manipal Hospital Whitefield