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To study the pain relief of two techniques (regional anaesthetic) after surgery (decompression) on lower vertebral column (lumber).

Comparison of Retrolaminar block and Erector spinae plane block for post-operative analgesia in patients undergoing lumbar spine decompression surgery A prospective randomized controlled trial. - NIL

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076170
Enrollment
84
Registered
2024-11-04
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Retrolaminar Block: All Patients will receive ultrasound guided B/L Retrolaminar block with 15 ml 0.375% Ropivacaine on either side and will be followed for analgesia using Numeric rati

Sponsors

AIIMS JODHPUR
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult Patients of either sex, aged between 18 to 65 years, belonging to ASA physical status 1 or 2, and scheduled for elective lumbar spine decompression surgery.

Exclusion criteria

Exclusion criteria: 1. Pregnant or lactating female. 2. History of bleeding diathesis or receiving anticoagulant treatment. 3. Skin infection at the site of the block area. 4. Patients with baseline cognitive deficits sufficient to make objective pain assessment unreliable. 5. Opioid-dependent or chronic analgesic abuse. 6. Patients with known allergy to amide local anaesthetic or opioid.

Design outcomes

Primary

MeasureTime frame
The primary outcome of our study will be to compare postoperative pain score using Numeric Rating Scale (NRS) in GROUP RLB & GROUP ESPB.Timepoint: During the first 24 hours after surgery

Secondary

MeasureTime frame
1. To compare the time to first rescue analgesic requirement. 2. To compare total analgesic consumed during the first 24 hrs after surgery. 3. To compare the intraoperative analgesic consumption. 4. To assess patient satisfaction score using Likert’s scale of both techniques. 5. To compare the side effects of both techniques. Timepoint: During the first 24 Hours in the Postoperative period

Countries

India

Contacts

Public ContactAnju Raja

Department of Anaesthesiology and Critical Care, AIIMS Jodhpur

drmsadik@gmail.com9414849733

Outcome results

None listed

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