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临床试验/NCT01751958
NCT01751958已完成3 期

Phase 3 Study of Evaluate Radiation Exposure and Procedure Times for Continuous Fluoroscopic Monitoring During Lumbar ESI

Seoul National University Bundang Hospital1 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2011年7月1日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
已完成
入组人数
1,000
试验地点
1
主要终点
Radiation dose

研究概览

简要总结

Evaluate radiation exposure and procedure times for continuous fluoroscopic monitoring during lumbar ESI

详细描述

The purpose of this prospective study was to evaluate radiation exposure and procedure times for fluoroscopic monitoring during lumbar ESI with analyzing the differences among operators (experienced staff and trainee) and among different method for ESI.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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
是

入选标准

  • •Suspected of having radiculopathic low back pain

排除标准

  • •Angiography is contraindicated

研究组 & 干预措施

Epidural Steroid injection

Experimental

Group-Epidural Steroid injection (Intermittent)

干预措施: Epidural steroid injection (Radiation)

Epidural Steroid Injection2

Experimental

Group-injection under angiography (continuous)

干预措施: Epidural steroid injection (Radiation)

结局指标

主要结局

Radiation dose

时间窗: Treatment on the day

Radiation dose of patients with spine invervention under angiography

次要结局

未报告次要终点

研究者

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

Suyoung Kim

Researcher

Seoul National University Bundang Hospital

研究点 (1)

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