Efficacy of retrolaminar and paravertebral block for postoperative analgesia in percutaneous nephrolithotomy patients - A double-blinded randomized controlled trial
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 104
- 试验地点
- 1
- 主要终点
- Duration of postoperative anlagesia provided by retrolaminar block verus paravertebral block in patients undergoing percutaneous nephrolithotomy
研究概览
简要总结
This double blinded randomized controlled trial aims to compare the postoperative analgesic efficacy of ultrasound guided retrolaminar block and paravertebral block in patients undergoing percutaneous nephrolithotomy under spinal anesthesia. After detailed preanesthetic evaluation, patients will be randomized into two groups: Group A - receiving RLB at the T10 level and Group B- receieving PVB at the T10 level , each with 20ml of 0.25% bupivacaine following saline confirmation of needle placement . All patients will receive standard anesthesia. Postoperatively, pain will be asssessed using the Visual Analog scala (VAS) at regular intervals over 24 hours by an independent blinded observer. The primary outcome is the duration of postoperative analgesia, defined as the time to first rescue anlagesia, while secondary outcomes include pain scores, total rescue analgesia consumption, and block related complications.
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
- 20.00 Year(s) 至 70.00 Year(s)(—)
- 性别
- All
入选标准
- •ASA PS I, II and III
- •Patient posted for elective PCNL.
排除标准
- •patient not giving consent obesity allergy to drugs.
结局指标
主要结局
Duration of postoperative anlagesia provided by retrolaminar block verus paravertebral block in patients undergoing percutaneous nephrolithotomy
时间窗: first 24 hours
次要结局
- Pain scores(postoperative period first 24 hours)
- Total rescue analgesic consumption(postoperative period first 24 hours)
- Block related complications(postoperative period first 24 hours)
研究者
Dharshini K
Sri Manakula Vinayagar medical College and Hospital
