Comparing pain relief methods using erector spinae plane block
Comparison of Pain Relief and Peripheral Perfusion Index Using Different Volume of Erector Spinae Plane Block
NA · Keimyung University Dongsan Medical Center · NCT06471907
This study is testing different amounts of local anesthetic used in a specific pain relief technique to see how well it works for people undergoing surgery or dealing with chronic pain.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 64 (estimated) |
| Ages | 20 Years to 80 Years |
| Sex | All |
| Sponsor | Keimyung University Dongsan Medical Center (other) |
| Locations | 1 site (Daegu) |
| Trial ID | NCT06471907 on ClinicalTrials.gov |
What this trial studies
This study aims to compare the effectiveness of different volumes of local anesthetics in providing pain relief and assessing the peripheral perfusion index during the erector spinae plane block (ESPB) procedure. ESPB is a less invasive alternative to traditional neuraxial anesthetic techniques, targeting an interfascial plane away from the spinal cord. The study will evaluate the pain control effectiveness of ESPB in various surgical contexts, including thoracic and abdominal surgeries, as well as its application in chronic pain conditions. By examining the physical spread of the anesthetic agent, the study seeks to enhance understanding of the ESPB's mechanism of action.
Who should consider this trial
Good fit: Ideal candidates include patients with lumbar disc herniation, foraminal stenosis, central stenosis, or spondylolisthesis experiencing significant back pain.
Not a fit: Patients with allergies to local anesthetics, pregnancy, spine deformities, or a history of lumbar spine surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved pain management techniques for patients undergoing various surgical procedures.
How similar studies have performed: Previous studies have shown promising results with the erector spinae plane block approach, indicating its potential effectiveness in pain management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * lumbar disc herniation * lumbar foraminal stenosis * lumbar central stenosis * lumbar spondylolisthesis * numerical rating scale \> 4 * back pain functional scale \< 45 * duration of pain \> 1 mon * patients who can fully understand all items described in back pain functional scale Exclusion Criteria: * Allergy to local anesthetics or contrast medium * Pregnancy * Spine deformity * Prior history of lumbar spine surgery * No previous lumbar MRI or CT * Patients with coagulation abnormality
Where this trial is running
Daegu
- Hong ji HEE — Daegu, South Korea (RECRUITING)
Study contacts
- Study coordinator: Ji H Hong
- Email: swon13@daum.net
- Phone: 01046794343
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Erector Spinea Plane Block