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Detection of Intravascular Injection Between Blunt and Sharp Needles During Cervical Transforaminal Epidural Block.

K

Kyungpook National University

Status

Completed

Conditions

Radicular; Neuropathic, Cervical
Pain

Treatments

Procedure: block with sharp-type block needle.
Procedure: block with Blunt-type block needle.

Study type

Interventional

Funder types

Other

Identifiers

NCT03286946
2016-09-009

Details and patient eligibility

About

This study evaluates the incidence of intravascular injection during cervical transforaminal epidural block using blunt needle, compared to the sharp needle. The investigators will performed cervical transforaminal epidural block using blunt-type block needle in half of participants or sharp-type block needle in the other half.

Full description

Cervical transforaminal epidural block is an effective treatment option of radiating pain. There are potential risks associated with transforaminal epidural block such as infection, dural puncture, bleeding, and intravascular injection. Although the risk is low, intravascular injection should be carefully monitored because intravascular injection of particulate steroids can cause fatal neurologic deficits such as spinal infarction and cerebral infarction.

The incidence of intravascular injection during transforaminal epidural block with real time fluoroscopy guidance depends on spinal level. The previous studies using real time fluoroscopy demonstrated that the incidence of intravascular injection of cervical transforaminal epidural block is higher than that of lumbosacral transforaminal epidural block.

In this study, therefore, the investigators investigate the incidence of intravascular injection during cervical transforaminal epidural block using blunt needle, compared to the sharp needle.

Enrollment

108 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with radiating pain from cervical spinal stenosis and herniated nucleus pulposus.

Exclusion criteria

  • Pregnancy, allergic to contrast media, patient refusal, and patients with persistent contraindication to nerve block such as coagulopathy and infection of the injection site.

Trial design

Primary purpose

Screening

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

108 participants in 2 patient groups

Blunt-type block needle
Experimental group
Description:
block with Blunt-type block needle.
Treatment:
Procedure: block with Blunt-type block needle.
Sharp-type block needle
Active Comparator group
Description:
block with Sharp-type block needle.
Treatment:
Procedure: block with sharp-type block needle.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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