To determine the effect of bilateral ultrasound - guided erector spinae plane block for postoperative analgesia in lumbar spine surgery

A prospective randomised controlled study to determine the effect of bilateral ultrasound - guided erector spinae plane block for post operative analgesia in lumbar spine surgery - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061081

Enrollment

Registered

2024-01-02

Start date

Unknown

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Erector spinae plane block: 15 ml each of 0.25% Bupivacaine erector spinae plane block given bilaterally in lumbar spine surgery Control Intervention1: Intravenous Analgesic: 15mg/kg in

Eligibility

Inclusion criteria

Inclusion criteria: American society of Anestheiologists 1 to 3

Exclusion criteria

Exclusion criteria: Refusal of consent Chronic analgesic therapy Those receiving anticoagulation Any history of bleeding disorder Allergic to local anaesthetics

Design outcomes

Primary

Measure	Time frame
Time to request first rescue analgesiaTimepoint: Pain score assessed from post extubation, 30 minutes, hourly up to 2 hour, then 2 hourly up to 4 hour and 4th hourly till 24hrs	—

Secondary

Measure	Time frame
Number of rescue analgesia usedTimepoint: Number oof dose assessed from post extubation 12th hourly for 24 hour	—

Countries

India

Contacts

Public ContactDr Thamarai Selvi

Sri Ramachandra Institute of Higher Education And Research

thames25@gmail.com9841552333

Outcome results

None listed

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