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临床试验/CTRI/2024/06/069481
CTRI/2024/06/069481尚未招募4 期

A Randomized Control Trial Comparing the Efficacy of Ultrasound Guided Erector Spinae Plane Block with Thoracolumbar Interfacial Plane Block For Lumbar Spine Surgeries.

SRM medical college hospital and research centre1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年6月30日最近更新:

试验速览

阶段
4 期
状态
尚未招募
入组人数
60
试验地点
1
主要终点
To compare the duration of post operative analgesia between the two blocks.

研究概览

简要总结

A total of 60 patients between 18-65yrs of asa1and asa2 undergoing elective lumbar spine surgeries will be prospectively studied in this single blinded randomised control trial.A total of 60 patients will be allocated into two groups group E and group T.Group E will receive usg guided erector spinae plane block and group T will receive usg guided thoracolumbar interfacial plane block.Both groups will receive block with 40ml of 0.375% ropivacaine,20ml on each side.All the patients will be assessed for primary outcome of post operative pain.Data collection will be done by observation and measurement of various parameters.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

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 1and 2 patients.
  • Age 18 to 65 yrs 3)patients of either sex 4)Patients who are undergoing elective lumbar spine surgeries.

排除标准

  • Patients refusal.
  • ASA 3 and 4 Patients 3)Patients with deranged coagulation profile 4)patients allergic to local anaesthetics.

结局指标

主要结局

To compare the duration of post operative analgesia between the two blocks.

时间窗: To compare the duration of post operative analgesia between the two blocks.Baseline,post intubation,10mins,20mins,30mins,40mins,50mins,60mins,70mins,80mins,90mins,100mins,110mins,120mins

次要结局

  • The number of doses of analgesics consumed in 24hrs.(4hrs post op to 24hrs)

研究者

申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Manisha Ratnam

Srm medical college hospital and research centre

研究点 (1)

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