Erector Spinae Plane Block in Oblique Lumbar Interbody Fusion Surgery

Intraoperative Fluoroscopic-guided Erector Spinae Plane Block in Oblique Lumbar Interbody Fusion Surgery

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0005938

Enrollment

Registered

2021-03-02

Start date

2021-02-16

Completion date

Unknown

Last updated

2021-03-22

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

Conditions

None listed

Interventions

Drug, Procedure/Surgery : 1. In the ESPB group, we inject 20cc of 0.5&#37

ropivacaine based on the C-arm guided image as the medial point of the ventral body&#39

s transverse process within 2-levels upstream from the fusion level. 2. In the placebo group, we inject 20cc normal saline at the same target point.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients performing one spinal level OLIF surgery. age 20 to 75 years old American Society of Anesthesiologists (ASA) physical status of 1–3

Exclusion criteria

Exclusion criteria: Previous spinal surgery Bleeding tendency or anticoagulation Allergic reaction to the contrast agent Allergic reaction to the local anesthetic agent Chronic usage of narcotic painkillers Functional conditions that are unable to walk due to paralysis of the lower extremities Impossible to assess pain due to communication difficulties If the patient refuses or does not agree to participate Severe liver disease, kidney disease, arrhythmia patients (risks for using ropivacaine)

Design outcomes

Primary

Measure	Time frame
Numeric rating scale of pain	—

Secondary

Measure	Time frame
Opioid consumption;6m gait speed	—

Countries

Korea, Republic of

Contacts

Public ContactDougho Park

POHANG STROKE AND SPINE HOSPITAL

Outcome results