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Erector Spinae Regional Anesthesia for Pain Control

The University of Texas System (UT) logo

The University of Texas System (UT)

Status and phase

Enrolling
Early Phase 1

Conditions

Pain Management

Treatments

Drug: Bupivacaine Injection

Study type

Interventional

Funder types

Other

Identifiers

NCT05794828
HSC20220911H

Details and patient eligibility

About

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

Full 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.

Enrollment

40 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Erector Spinae Plane Block (ESP) administration
Experimental group
Description:
Patients with the listed diagnoses will be offered and then consented for an ESPB under ultrasound guidance.
Treatment:
Drug: Bupivacaine Injection

Trial contacts and locations

4

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Central trial contact

Morgan Ritz, MD

Data sourced from clinicaltrials.gov

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