Opioid free anaesthesia in lumbar microscopic discectomy and comparing bilateral erector spinae plane block and intravenous lignocaine infusion for post operative pain management

Comparison between the efficacy of erector spinae plane block and intravenous lidocaine infusion on post-operative pain outcomes in opioid free anaesthesia after lumbar disc surgeries - NIL

Status

Active, not recruiting

Phases

Phase 3Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061553

Enrollment

Registered

2024-01-18

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: O- Medical and Surgical

Interventions

Intervention1: Erector Spinae plane block: Patients will be given Bilateral erector spinae plane block (ESPB) with levobupivacaine 20ml (0.25%) at L3 level + PCA morphine (bolus of morphine 1mg will b

Eligibility

Inclusion criteria

Inclusion criteria: 1)Age 18-65 years 2)All patients giving written consent will be taken for study 3)American Society of Anaesthesiology physical status grade 1 to 3

Exclusion criteria

Exclusion criteria: 1)Allergy to local anaesthetic drug or any other drug used in the study 2)MI within 6 months, profoundly decreased LVEF( 3)Severe liver disease(AST OR ALT or bilirubin >2.5 times the upper limit of normal) 4)Renal failure(creatinine outside normal range) 5)Patients who cannot operate PCA pump 6)Chronic use of opioids and beta blockers 7)Chronic pain syndromes 8)Inability to understand pain assessment 9)Pregnancy and lactation 10)Severe mental impairment, known psychiatric illness

Design outcomes

Primary

Measure	Time frame
To assess the post-operative pain outcome using numerical rating scale (NRS) after erector spinae plane block and intravenous lignocaine infusion and its comparison with the control group in microscopic lumbar discectomyTimepoint: To assess the post-operative pain outcome using numerical rating scale (NRS) after erector spinae plane block and intravenous lignocaine infusion and its comparison with the control group in microscopic lumbar discectomy at 0, at. 30 minutes,1,2,3,4,5,6,8,10,12,16,20,24 hours	—

Measure

Time frame

To assess the post-operative pain outcome using numerical rating scale (NRS) after erector spinae plane block and intravenous lignocaine infusion and its comparison with the control group in microscopic lumbar discectomyTimepoint: To assess the post-operative pain outcome using numerical rating scale (NRS) after erector spinae plane block and intravenous lignocaine infusion and its comparison with the control group in microscopic lumbar discectomy at 0, at. 30 minutes,1,2,3,4,5,6,8,10,12,16,20,24 hours

—

Secondary

Measure	Time frame
To assess the quality of recovery and post-operative outcome using QOR-15 score and S-DN4 questionnaireTimepoint: QOR-15 score will be assessed preoperatively, postoperatively and at 3 Months S-DN4 questionnaire will be assessed at 3 months	—

Countries

India

Contacts

Public ContactShreya Sharma

Himalayan institute of medical sciences, Jollygrant, Dehradun

gurjeetkhurana@srhu.edu.in9410539190

Outcome results

None listed

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