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Erector Spinae Plane Block vs. Usual Care for ED Patients With Mechanical Back Pain

I

Island Health

Status

Completed

Conditions

Back Pain

Treatments

Drug: Usual care
Procedure: Erector Spinae plane block using 20 ml of bupivicaine 0.25%

Study type

Interventional

Funder types

Other

Identifiers

NCT05982483
C2018-102

Details and patient eligibility

About

The goal of this clinical trial is to compare the Erector Spinae plane (ESP) block, a nerve block, to usual care in emergency department patients with back pain. The main question it aims to answer:

Is the ESP block superior to usual care in the treatment of back pain in the emergency department? Participants will be randomly assigned to the ESP or the usual care group. Pain improvement at the time of emergency department discharge will be compared.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: Patients deemed to have mechanical back pain with a component of paravertebral tenderness or paravertebral spasm reported by the patient or noted on examination by treating physician.

Exclusion Criteria:

  • previous recipient of erector spinae plane block
  • exam concerning for cauda equina syndrome
  • current IV drug use
  • organ transplant recipient
  • history of or suspected bleeding diathesis
  • current use of anticoagulants
  • sepsis or soft tissue infection at site of the block within last three months
  • pregnancy
  • overt malignancy involving skin or underlying soft tissue at the site of block
  • allergy to any of the research medications
  • inability to participate in telephone follow-up

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

ESP cohort
Experimental group
Description:
Randomized to receive the ultrasound-guided ESP block.
Treatment:
Procedure: Erector Spinae plane block using 20 ml of bupivicaine 0.25%
Usual care cohort
Active Comparator group
Description:
Randomized to usual care as dictated by the treating emergency physician
Treatment:
Drug: Usual care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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