Actively Recruiting
Comparison of Pain Relief and Peripheral Perfusion Index
Led by Keimyung University Dongsan Medical Center · Updated on 2024-07-05
64
Participants Needed
1
Research Sites
45 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary endpoint of this study is to compare the pain relief and peripheral perfusion index using different volume of local anesthetics in erector spinae plane block.
CONDITIONS
Official Title
Comparison of Pain Relief and Peripheral Perfusion Index
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of lumbar disc herniation, lumbar foraminal stenosis, lumbar central stenosis, or lumbar spondylolisthesis
- Numerical rating scale score greater than 4
- Back pain functional scale score less than 45
- Pain duration longer than 1 month
- Ability to fully understand all items in the back pain functional scale
You will not qualify if you...
- Allergy to local anesthetics or contrast medium
- Pregnancy
- Presence of spine deformity
- Prior history of lumbar spine surgery
- No previous lumbar MRI or CT scan
- Coagulation abnormality
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Hong ji HEE
Daegu, South Korea, 42601
Actively Recruiting
Research Team
J
Ji H Hong
CONTACT
J
Ji Hoon Park
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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