Comparison of Pain Relief and Peripheral Perfusion Index
ConditionErector Spinea Plane Block
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-80
SponsorKeimyung University Dongsan Medical Center
About this trial
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.
Eligibility criteria
Qualifiers
lumbar disc herniation
lumbar foraminal stenosis
lumbar central stenosis
lumbar spondylolisthesis
Disqualifiers
Allergy to local anesthetics or contrast medium
Pregnancy
Spine deformity
Prior history of lumbar spine surgery
Trial design
Treatments tested in this trial
- erector spinae plane block
Treatment groups
64 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov