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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05723354
Other study ID # 2023-01-025-05
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 13, 2023
Est. completion date November 30, 2023

Study information

Verified date February 2023
Source Keimyung University Dongsan Medical Center
Contact Ji H Hong
Phone 01046794343
Email swon13@daum.net
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary endpoint of this study was to compare the clinical efficacy of axillary block in patients of cervical radiculopathy using 2 volumes of local anesthetics.


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 interfascial plane injection was performed in patients with cervical radiuculopathy. There is no study showing clinical efficacy of interfascial plane injection of axillary block in patients of cervical radiculopathy.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date November 30, 2023
Est. primary completion date November 30, 2023
Accepts healthy volunteers No
Gender All
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: - Cervical foraminal stenosis - Cervical central stenosis - Cervical disc herniation - Cervical spondylolisthesis - Prominent arm pain rather than neck pain Exclusion Criteria: - Infection - Pregnancy - allergy to local anesthetic agents - previous cervical spine surgery - Prominent neck pain rather than arm pain

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
axillary block guided by ultrasound
axillary block using local anesthetics

Locations

Country Name City State
Korea, Republic of Hong ji HEE Daegu

Sponsors (1)

Lead Sponsor Collaborator
Keimyung University Dongsan Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numerical rating scale changes among 4 time periods Numerical rating scale changes among 4 time periods baseline, 2 weeks after injection, 4 weeks after injection, 8 weeks after injection
Primary Neck disability injex changes between 2 time periods Neck disability injex changes between 2 time periods baseline, 8 weeks after injection
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