- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05723354
Clinical Efficacy of Axillary Block in Cervical Radiculopathy
Comparison of Clinical Efficacy of Axillary Block in Patients of Cervical Radiculopathy
Study Overview
Status
Conditions
Intervention / Treatment
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 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.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Daegu, Korea, Republic of, 42601
- Recruiting
- Hong ji HEE
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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 Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: 5ml axillary block group
interfascial plane axillary block group using 5 ml local anesthetics
|
axillary block using local anesthetics
|
Active Comparator: 10ml axillary block group
interfascial plane axillary block group using 10 ml local anesthetics
|
axillary block using local anesthetics
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Numerical rating scale changes among 4 time periods
Time Frame: baseline, 2 weeks after injection, 4 weeks after injection, 8 weeks after injection
|
Numerical rating scale changes among 4 time periods
|
baseline, 2 weeks after injection, 4 weeks after injection, 8 weeks after injection
|
Neck disability injex changes between 2 time periods
Time Frame: baseline, 8 weeks after injection
|
Neck disability injex changes between 2 time periods
|
baseline, 8 weeks after injection
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023-01-025-05
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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