Clinical Trials Directory

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

TypeNameDescription
DRUGBupivacaine InjectionBucivacaine 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

Source: ClinicalTrials.gov record NCT05794828. Inclusion in this directory is not an endorsement.