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临床试验/NCT02750436
NCT02750436已完成不适用

A Prospective Randomized Comparison of Ultrasound Versus Fluoroscopic Guidance for Sacral Lateral Branch Blocks

Montreal General Hospital2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年4月25日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Performance time

研究概览

简要总结

Sacral lateral branch blocks are used for the diagnosis and treatment of sacroiliac joint pain. This study will compare ultrasound and fluoroscopy guidance for sacral lateral branch blocks. Outcomes examined will include performance times and success rates.

研究设计

研究类型
Interventional
分配方式
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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any consenting patient over 18 years of age, undergoing a diagnostic sacral lateral branch block for suspected sacroiliac joint related pain.

排除标准

  • Inability to consent, iodine or lidocaine allergy, pregnancy, coagulopathy (as defined by an international normalized ratio over 1.4, platelets under 100,000, or a documented bleeding disorder) and inability to visualize the target areas necessary for sensory testing (posterior superior iliac spine, dorsal aspect of SIJ) under ultrasound guidance.

结局指标

主要结局

Performance time

时间窗: Duration of procedure (less than 20 minutes)

Block performance time will be measured from the time the first image is acquired, until the last injection is completed. Typical performance time are expected to be less than 20 minutes for both groups.

次要结局

  • Change in pain numerical rating score from baseline(Baseline and 20 minutes after procedure)

研究者

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

Roderick Finlayson

Professor Department of Anesthesia

Montreal General Hospital

研究点 (2)

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