Trials / Completed
CompletedNCT05794828
Erector Spinae Regional Anesthesia for Pain Control
Erector Spinae Regional Anesthesia for Pain Control in the Emergency Department
- Status
- Completed
- Phase
- EARLY_Phase 1
- Study type
- Interventional
- Enrollment
- 15 (actual)
- Sponsor
- The University of Texas Health Science Center at San Antonio · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine Injection | Bucivacaine will be administered intramuscularly according to package insert directions after first numbing the area with lidocaine subcutaneously |
Timeline
- Start date
- 2023-09-15
- Primary completion
- 2025-02-18
- Completion
- 2025-02-18
- First posted
- 2023-04-03
- Last updated
- 2025-08-27
Locations
4 sites across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05794828. Inclusion in this directory is not an endorsement.