Clinical Trials Directory

Trials / Completed

CompletedNCT05031936

: Intravascular Injection Rates During Cervical Medial Branch Block

Comparison of Intravascular Injection Rates During Cervical and Lumbar Medial Branch Block Using Touhy or Quincke Type Needle

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
67 (actual)
Sponsor
Keimyung University Dongsan Medical Center · Academic / Other
Sex
All
Age
20 Years – 79 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare using Toughy needle has an advantage of reducing intravascular injection rates during cervical medial branch block.

Detailed description

In previous reports, the use of Toughy needle was thought to reduce the incidence of intravascular injection as low as 2.9% during lumbar transforaminal injection. Blunt needles with a pencil point tip, such as Whitacre needles, are not as sharp at their tip as are Quincke needles, which have bevels. Toughy or blunt needles may therefore be less likely to penetrate a vessel during a procedure. Hence, we postulated the incidence of intravenous uptake would be significantly lower using a Toughy needle than using a Quincke needle for lumbar medial branch block. To confirm the intravascular injection rates, we used the real time fluoroscopy after injection of contrast medium. The goal of this study was to compare the incidence of intravascular injection rate betweeen Toughy and Quincke needles using real time fluoroscopy during cervical medial branch block

Conditions

Interventions

TypeNameDescription
PROCEDUREcervical spinal injection with 0.2% ropivacainespinal injections performed in cervical pillar area to relieve chronic neck pain

Timeline

Start date
2021-08-12
Primary completion
2022-10-30
Completion
2022-10-30
First posted
2021-09-02
Last updated
2022-12-20

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT05031936. Inclusion in this directory is not an endorsement.