Want to study effect of intravenous lignocaine in post operative pain in spine surgery

A Randomized Controlled Study To Evaluate The Effect Of Intraoperative Intravenous Lignocaine Infusion On Early Postoperative Pain After Elective Lumbar Spine Surgeries At SMS Medical College And Hospital Jaipur - NIL

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/04/107570

Enrollment

Registered

2026-04-06

Start date

Unknown

Completion date

Unknown

Last updated

2026-04-27

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: Lignocaine: 60 mg intravenous before surgery and 90 mg intravenous infusion just before end of surgery, effect seen up to 24 hour post surgery Control Intervention1: Saline: Used as bli

Eligibility

Inclusion criteria

Inclusion criteria: Patient undergoing elective Lumbar spine surgery with informed written consent Patients of either gender with age group ranging from 25 to 60 years. ASA grade I and II

Exclusion criteria

Exclusion criteria: Patients with a known history of hepatic or renal dysfunction, atrio-ventricular block. History of hypersensitivity to study medication. Patients having history of previous back surgery Patient with history of drug abuse

Design outcomes

Primary

Measure	Time frame
Mean time to demand first rescue analgesia Mean rescue analgesic consumption Mean NRS value Proportion of patients experiencing side effects Mean haemodynamic parameters( HR, SBP, DBP, MBP)Timepoint: 15 Min,30 min,45 min,60 min	—

Secondary

Measure	Time frame
nilTimepoint: nil	—

Countries

India

Contacts

Public ContactRashi Agarwal

Sms Medical College And Hospital

drneelu13@gmail.com9782480455

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026