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临床试验/CTRI/2025/09/094863
CTRI/2025/09/094863尚未招募不适用

Comparison of Ultrasound guided modified thoracolumbar interfascial plane block versus erector spinae plane block for pain relief among patients undergoing spine surgery

R Keerthana1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2025年10月3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
48
试验地点
1
主要终点
To compare postoperative level of pain using VAS score between ultrasound guided modified thoracolumbar interfascial plane block and ultrasound guided erector spinae plane block among patients undergoing spine surgery

研究概览

简要总结

This study is a randomized, double blinded, parallel group, single-centre trial comparing ultrasound guided modified Thoracolumbar interfascial plane block with ultrasound guided Erector spinae plane block for pain relief in patients undergoing spine surgery. The primary outcome is to compare the postoperative pain scores at six defined time points between two groups. The secondary outcomes will be to compare intraoperative and postoperative ( first 24 hours) total opioid consumption, time to first rescue analgesia and patient satisfaction scores.

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
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients with ASA physical status I and II scheduled for lumbar level laminectomy or lumbar level decompression with or without posterior instrumentation.

排除标准

  • Patients with BMI more than 30kg/m2
  • Patients with Coagulopathy
  • Patients with local site infections
  • Patients who are allergic to local anesthetic drugs
  • Patient with psychiatric problems
  • Patients with neurological and neuromuscular disorders.

结局指标

主要结局

To compare postoperative level of pain using VAS score between ultrasound guided modified thoracolumbar interfascial plane block and ultrasound guided erector spinae plane block among patients undergoing spine surgery

时间窗: Pain will be measured at 0, 2, 4, 8, 16 and 24 hours postoperatively

次要结局

  • To compare the total opioid consumption in intraoperative period between the two groups(Intraoperative period)
  • To compare the total opioid consumption in the postoperative period between the two groups(Postoperative period ( first 24 hours ))
  • To compare the time to first rescue analgesia between the two groups(Postoperative period ( first 24 hours ))
  • To compare the patient satisfaction score between the two groups(Postoperative period ( at the end of 24 hours ))

研究者

发起方
R Keerthana
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

R Keerthana

Jawaharlal Institute of Postgraduate Medical Education and Research ( JIPMER )

研究点 (1)

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