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A study to evaluate the effect of a pain relief injection (Erector Spinae Plane Block) on postoperative pain and recovery in patients undergoing endoscopic surgery for slipped lumbar disc.

A RANDOMISED CONTROLLED STUDY TO ASSESS THE EFFICACY OF ULTRASOUND GUIDED ERECTOR SPINAE PLANE BLOCK IN BIPORTAL ENDOSCOPIC LUMBAR DISCECTOMY - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/06/111995
Enrollment
50
Registered
2026-06-04
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-22

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 Health Condition 2: M438- Other specified deforming dorsopathies

Interventions

Intervention1: Bilateral ultrasound guided erector spinae plane block with ropivacaine: Patients will receive bilateral ultrasound guided erector spinae plane block using 20 ml of 0.25 percent ropivac

Sponsors

Jawaharlal Nehru Medical College, Aligarh Muslim University
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: American Society of Anesthesiologists (ASA) class I-II Single level lumbar disc herniation/ stenosis scheduled for biportal endoscopic lumbar discectomy.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intraoperative opioid consumption in morphine milligram equivalents (MME) Timepoint: From induction of anesthesia to completion of surgery—

Secondary

MeasureTime frame
Sedation-related adverse events (Intra-op) - Using the World SIVA Sedation Adverse Event Reporting Tool (type, timing, severity, interventions) in two study groups E & C. Timepoint: Assessed continuously during the intraoperative period, from administration of study intervention until completion of surgery.;Time to first rescue analgesic (Post-Op) in two study groups E & C. Timepoint: Assessed from completion of surgery until administration of first rescue analgesic, up to 24 hours postoperatively.;Post-operative sedation level by RASS (Richmond Agitation-Sedation Scale) in two study groups E & C. Timepoint: Assessed at 0, 2, 4, 6, 12, & 24 hours after surgery.;Post-operative pain intensity on NRS (Numerical Rating Scale) 0 10 at 0, 2, 4, 6, 12, 24 hours after surgery in two study groups E & C. Timepoint: Assessed at 0, 2, 4, 6, 12, & 24 hours after surgery.;Block-related complications in two study groups E & C. Timepoint: Assessed from block administration until 24 hours postoperatively.—

Countries

India

Contacts

Public ContactObaid Ahmed Siddiqui

Jawaharlal Nehru Medical College, Aligarh Muslim University

obaidahmad2008@gmail.com9897695761

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 29, 2026