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Prediction of Clinical Outcome in Axillary Block

K

Keimyung University

Status

Enrolling

Conditions

Pain, Chronic

Treatments

Procedure: axillary block using 5 ml local anesthetics

Study type

Observational

Funder types

Other

Identifiers

NCT05723419
20201-025-04

Details and patient eligibility

About

The primary endpoint of this study was to identify that Perfusion index (PI) has any predictive value for the treatment outcome of cervical radiculopathy

Full description

The interscalene brachial plexus block is an effective intervention for reducing postoperative pain but is related to side effects, Suprascapular nerve block and a block of the axillary nerve have been introduced as alternatives to the interscalene brachial plexus for the control of postoperative pain. Previous study demonstrated new method of axillary block using interfascial plane injection guided by ultrasoud. Axillary block has been used widely for the relief of postoperative arm pain.

Recent study deomonstrated good pain relief when ultrasound guided fascial plane injection was performed in patients with cervical radiuculopathy.

The perfusion index (PI) is a numerical value for the ratio between pulsatile and non-pulsatile blood flow measured by a special pulse oximeter. Although the special probe for PI measurement is relatively more expensive compared with ordinary pulse oximetery probes, its benefit as a marker of peripheral perfusion and as an idex for sympathetic stimulation have increased its use progressively. PI has been used widely for the prediction of success of brachial plexus block or axillary block. Changes of PI ratio value showed an excellent predictive value for the success of block.

There have been no studies demonstrating any predictive value of PI in axillary block for the relief of cervical radiulopathy

Enrollment

70 estimated patients

Sex

All

Ages

20 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cervical foraminal stenosis
  • Cervical central stenosis
  • Cervical disc herniation
  • Cervical spondylolisthesis

Exclusion criteria

  • Infection
  • pregnancy
  • allergy to local anesthetic agents
  • previous cervical spine surgery

Trial contacts and locations

1

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Central trial contact

Ji Hoon Park; Ji H Hong

Data sourced from clinicaltrials.gov

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