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临床试验/CTRI/2023/07/054776
CTRI/2023/07/054776尚未招募不适用

Comparison of Bupivacaine and Ropivacaine in Ultrasound-guided bilateral erector spine plane block for post-operative analgesia in lumbar spine surgery

ABVIMS and Dr.RML Hospital1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2023年7月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Duration of postoperative analgesia,time between institution of block and requirement of first rescue analgesia

研究概览

简要总结

To compare the efficacy of bupivacaine and ropivacaine in ultrasound guided erector spinae block for providing post operative analgesia in lumbar spine surgery

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • ASA Grade I and II,Patients posted for lumbar spine surgery.

排除标准

  • Patients not consenting to the procedure Local infection at the block site Pre- existing coagulation disorders Allergy to local anesthetics (prior test dosing with Bupivacaine and ropivacaine will be given).

结局指标

主要结局

Duration of postoperative analgesia,time between institution of block and requirement of first rescue analgesia

时间窗: Before shifting to PACU | Immediately after shifting to PACU | 30 minutes | 1st hour | 1.5 hour | 2nd hour | 4th hour | 6th hour | 8th hour | 10th hour | 12 th hour

次要结局

  • Postoperative hemodynamic parameters(Post operative nausea vomiting and any other adverse effects)

研究者

发起方
ABVIMS and Dr.RML Hospital
申办方类型
Research institution and hospital

研究点 (1)

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