Effectiveness and safety of erector spinae plane block in post-op management of pain in patients undergoing lumbar spine surgery

Efficacy of Erector Spinae Plane Block in post-operative pain management of lumbar spine surgery - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/06/089141

Enrollment

Registered

2025-06-19

Start date

Unknown

Completion date

Unknown

Last updated

2025-06-24

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

Conditions

Health Condition 1: 4- Measurement and Monitoring Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Erector spinae plane block: Erector spinae plane block given by catheter in the Erector spinae plane inj. Ropivacaine 0.125% at rate of 10ml/hr Control Intervention1: IV opoid: IV fenta

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade I/II Informed consent to participate Patients undergoing lumbar spine surgery under general anaesthesia

Exclusion criteria

Exclusion criteria: Coagulopathy Pregnant females Sensitivity to local anaesthetics Age below 18yrs

Design outcomes

Primary

Measure	Time frame
Safety and efficacy of erector spinae plane block in post-op analgesia of lumbar spine surgery patientsTimepoint: Pre-op, 0hr (atextubation), 1hr,2hr,4hrs,6hrs,12hrs, 24hrs	—

Secondary

Measure	Time frame
Time to first rescue analgesia, total opoid consumption, hemodynamic changes at extubation, incidents of respiratory depression,PONV,LAST,loss of power, hypotensionTimepoint: 0-24hrs	—

Countries

India

Contacts

Public ContactVaishnavi

GSVM medical college

anil_16021976@rediffmail.co.in9336107410

Outcome results

None listed

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