Erector spina block in lumbar spinal surgery

The Efficacy of Ultrasound Guided Erector spina block in postoperative pain reduction in lumbar spinal surgeries

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20200628047936N1

Enrollment

Registered

2020-09-27

Start date

2020-09-05

Completion date

Unknown

Last updated

2020-10-06

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

Conditions

Pain control after spinal surgery. Other acute postprocedural pain

Interventions

Intervention 1: Intervention group:After induction of anesthesia and changing the position to prone the case group receive erector spina block under ultrasound guide with bupivacaine 0.25 % , 20 cc ea

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: All candidated 18-75 y/o patients for spinal lumbar surgery patients with normal hepatic and renal function ASA score 1-2

Exclusion criteria

Exclusion criteria: addiction BMI more than 35 or less than 16 allergy to local anesthetics mental disorders

Design outcomes

Primary

Measure	Time frame
Postop pain score in defined intervals. Timepoint: 1, 2 , 4, 6, 12, 24 Hours after surgery. Method of measurement: Pain scale chart (NRS).;Opioid consumption in first postop 24 hours. Timepoint: First 24 hours. Method of measurement: Amount of Opioid consumption recorded by nurse.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArash Tafrishinejad

Shahid Beheshti University of Medical Sciences

arashtafrishi@gmail.com+98 21 2273 4715

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026