Erector Spinae Regional Anesthesia for Pain Control
- Registration Number
- NCT05794828
- Brief Summary
Interventional study to use erector spinae plane block (ESPB) on diagnoses of posterior or lateral rib fractures, vertebral fractures, pancreatitis, pancreatic cancer, renal colic, and back pain for multimodal pain therapy to determine its assistance with pain relief as well as the patient's use of opiates after block completion
- Detailed Description
Patients with the listed diagnoses will be offered and then consented for an ESPB under ultrasound guidance. They will rate their pain before and 30 minutes after the procedure using the ordinal categorical data on a numeric pain scale. Total patient opiate use will be gathered up to 8 hours after block completion.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 40
- Posterior/lateral rib or vertebral fractures
- Pancreatitis or pancreatic cancer
- Renal colic
- Back pain
- Unstable vitals
- Infection or open wound over insertion site
- Prior allergic reaction to local anesthetic
- Pregnant females
- Patients <18 years old
- Altered mentation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Erector Spinae Plane Block (ESP) administration Bupivacaine Injection Patients with the listed diagnoses will be offered and then consented for an ESPB under ultrasound guidance.
- Primary Outcome Measures
Name Time Method Pain Scale Rating Baseline to study procedure end (approximately 30 minutes) Change in pain scale rating assessed by the participants on a scale from 0-10 with 0 indicating no pain and 10 indicating the most severe pain.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (3)
Crozer Chester Medical Center
🇺🇸Upland, Pennsylvania, United States
University Hospital
🇺🇸San Antonio, Texas, United States
Baylor Scott & White
🇺🇸Temple, Texas, United States