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临床试验/NCT07538765
NCT07538765已完成不适用

Efficacy of Transforaminal Epidural Steroid Injections in Lumbar Radicular Pain

Ankara City Hospital Bilkent1 个研究点 分布在 1 个国家目标入组 221 人开始时间: 2024年9月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
221
试验地点
1
主要终点
Visual analog scale

研究概览

简要总结

The goal of this retrospective study is to evaluate the effectiveness of transforaminal epidural steroid injections (TFESI) in patients with radicular low back pain caused by lumbar disc herniation who did not improve with conservative treatment.

The main questions it aims to answer are:

How effective is TFESI in reducing pain and improving physical function over a three-month period?

Can this procedure serve as a viable alternative to surgery for patients with persistent radiculopathy?

Participants aged 18 to 90 underwent image-guided injections and were monitored for three months. Researchers tracked changes in their pain levels (using the Visual Analog Scale) and their ability to perform daily activities (using the Oswestry Disability Index) to determine the treatment's success.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Other

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Between 18 and 90 years,
  • Presence of Low Back Pain with unilateral or bilateral pain radiating to the lower extremity,
  • Duration of symptoms for at least three months and unresponsive to conservative management,
  • Evidence of lumbar intervertebral disc herniation confirmed by MRI within the last six months

排除标准

  • Prior lumbar ESI within 3 months,
  • History of polyneuropathy or entrapment neuropathy,
  • Presence of bleeding diathesis,
  • Systemic or local infections,
  • Having systemic and rheumatic diseases associated with peripheral nerve involvement.

研究组 & 干预措施

patients with radicular low back pain caused by lumbar disc herniation

干预措施: transforaminal epidural steroid injections (TFESI) (Procedure)

结局指标

主要结局

Visual analog scale

时间窗: baseline, the 2nd weeks, and the 3rd months

(VAS: 0-10)

次要结局

  • functional status,(baseline, the 2nd weeks, and the 3rd months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Emine Esra Bilir

medical doctor

Ankara City Hospital Bilkent

研究点 (1)

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