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Clinical Trials/NCT05723419
NCT05723419
Recruiting
Not Applicable

Perfusion Index Value in Predicting the Clinical Outcome of Axillary Block

Keimyung University Dongsan Medical Center1 site in 1 country70 target enrollmentFebruary 13, 2023
ConditionsPain, Chronic

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Chronic
Sponsor
Keimyung University Dongsan Medical Center
Enrollment
70
Locations
1
Primary Endpoint
Perfusion index changes among 4 time periods
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

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

Detailed 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

Registry
clinicaltrials.gov
Start Date
February 13, 2023
End Date
November 30, 2023
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ji Hee Hong

Professor

Keimyung University Dongsan Medical Center

Eligibility Criteria

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

Outcomes

Primary Outcomes

Perfusion index changes among 4 time periods

Time Frame: baseline, 10 minutes, 20 minutes, 30 minutes after axillary block

Perfusion index changes among 4 time periods

Number of patients showing no reduction in numerical rating scale

Time Frame: 1 month after axillary block

Number of patients showing no reduction in numerical rating scale

Number of patients showing numerical rating scale reduction more than 50%

Time Frame: 1 month after axillary block

Number of patients showing numerical rating scale reduction more than 50%

Number of patients showing numerical rating scale reduction less than 50%

Time Frame: 1 month after axillary block

Number of patients showing numerical rating scale reduction less than 50%

Neck disability index changes between 2 time periods

Time Frame: baseline, 1 month after axillary block

Neck disability index changes between 2 time periods

Study Sites (1)

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