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临床试验/NCT04350307
NCT04350307已完成不适用

Differential Rates of Intravascular Uptake and Pain Perception During Lumbosacral Transforaminal Epidural Steroid Injection Using a 22-gauge Needle Versus 25-gauge Needle

Yale University2 个研究点 分布在 1 个国家目标入组 162 人开始时间: 2018年2月1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
162
试验地点
2
主要终点
Intravascular Uptake

研究概览

简要总结

The aim of the study was to quantify the difference between a 22-gauge needle and 25-gauge needle during lumbosacral epidural steroid injection in regards to intravascular uptake and pain perception. There is the notion that a smaller gauge needle may lead to less intravascular uptake and less pain.

详细描述

Inadvertent intravascular injection has been suggested as the most probable mechanism behind serious neurological complications during transforaminal epidural steroid injections. There is the notion that a smaller gauge needle may lead to less intravascular uptake and less pain. The aim of the study was to quantify the difference between a 22-gauge needle and 25-gauge needle during lumbosacral transforaminal epidural steroid injection in regards to intravascular uptake and pain perception.

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
Single (Participant)

盲法说明

Randomization was done separately for each provider based on a computer generated algorithm. Patients were blinded to the gauge of the needle used for the procedure.

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

  • patients with low back pain and/or radicular pain,
  • patients scheduled for lumbosacral TFESI.

排除标准

  • patients with contrast/local anesthetic allergy,
  • patients with pregnancy, coagulopathy, systemic infection, and inability to provide informed consent,
  • vulnerable patient population including prisoners,
  • patients with severe anxiety,
  • patients with prior lumbar surgery,
  • age <18 years old, and
  • Body Mass Index (BMI) > 40.

结局指标

主要结局

Intravascular Uptake

时间窗: During the procedure

The intravascular uptake percentage reported in the study is the percent of 'needles' that showed intravascular uptake. Hence higher 'intravascular uptake percentage' means worse outcome. The mean percentages were averaged across participants were compared between treatment arms. Presence or absence of intravascular uptake during live fluoroscopy and/or blood aspiration per needle. Once needle reached its target (epidural space), contrast was injected to confirm the presence or absence of intravascular uptake via live fluoroscopy or aspiration was attempted using a syringe to confirm the presence or absence of intravascular uptake. If contrast pattern suggested needle was in a vessel or blood was aspirated using a syringe, outcome measure was marked 'PRESENT'. If contrast pattern suggested needle was not in a vessel and no blood was aspirated using a syringe, outcome measure was marked 'ABSENT'. In other words, primary outcome measure was binary in nature.

次要结局

  • Patient Reported Pain(During the procedure)

研究者

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

Robin Raju, DO

Clinical Assistant Professor

Yale University

研究点 (2)

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