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Erector Spinae Regional Anesthesia for Pain Control

Erector Spinae Regional Anesthesia for Pain Control in the Emergency Department

Status
Completed
Phases
Early Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05794828
Enrollment
15
Registered
2023-04-03
Start date
2023-09-15
Completion date
2025-02-18
Last updated
2025-08-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain Management

Keywords

Erector spinae plane block, ESPB, Pain reduction

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.

Interventions

DRUGBupivacaine Injection

Bucivacaine will be administered intramuscularly according to package insert directions after first numbing the area with lidocaine subcutaneously

Sponsors

The University of Texas Health Science Center at San Antonio
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single group open label assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Posterior/lateral rib or vertebral fractures * Pancreatitis or pancreatic cancer * Renal colic * Back pain

Exclusion criteria

* Unstable vitals * Infection or open wound over insertion site * Prior allergic reaction to local anesthetic * Pregnant females * Patients \<18 years old * Altered mentation

Design outcomes

Primary

MeasureTime frameDescription
Pain Scale RatingBaseline 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.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026