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临床试验/CTRI/2022/07/043660
CTRI/2022/07/043660尚未招募不适用

Comparative study between Transforaminal Epidural Steroid Injection in patient versus High Volume Lumbar Erector Spinae Block in patient with Lowbackache and Radicular pain A Prospective Randomized Trial

IMS BHU1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年4月7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
30
试验地点
1
主要终点
Pain levels by Numeric rating scale (NRS)

研究概览

简要总结

Low back pain is the leading cause of activity limitation and work absence throughout much of the world and is associated with an enormous economic burden. Lifetime prevalence of LBP is estimated to be >70% in industrialized countries. The purpose of the current study is to perform a relative credible and comprehensive assessment to compare the efficiency and safety of transforaminal epidural steroid injection Versus high volume lumber Erector spinae block in patient with low backache and radicular pain.

The prospective study will be carried out on 60 adults patient which will be allocated into 2 groups containing 30 patient in each group.

Patient with unilateral low backache with radicular pain persisting medical treatment  were taken into study.

After which randomisation was done and primary outcome was noted by numeric rating scale.

Secondary outcome was also noted at 1month and 3 month.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Double Blind Double Dummy

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
All

入选标准

  • 1.ASA grade 1 and 2 2.Patient with low back ache with unilateral radicular pain persisting despite medical treatment.

排除标准

  • Patient refusal Coagulation disorders Allergic to Local Anesthetic agents Presence of infection at injection area Patient with previous history of spinal surgery Patient with co morbidities Spinal cord disease like scoliosis or mechanical instability like fracture More than 2 level of disc hernia Degenerated and sequestered disc.

结局指标

主要结局

Pain levels by Numeric rating scale (NRS)

时间窗: Immediately(With in 30 mins)

次要结局

  • Pain level after intervention at 1 month , 3 month by Numeric rating scale.(Oswestry disability index)

研究者

发起方
IMS BHU
申办方类型
Government medical college

研究点 (1)

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