Randomized comparison to study effect of lignocaine infusion as a part of analgesic regimen in Robotic lumbar spine surgery

Comparative study of intraoperative Intravenous lignocaine infusion as a part of the multimodal analgesic therapy in Robotic multilevel (2-3) lumbar fusion surgery- A Prospective Randomized Double Blinded Controlled trial - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/02/062900

Enrollment

142

Registered

2024-02-20

Start date

Unknown

Completion date

Unknown

Last updated

2026-03-30

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

Conditions

Health Condition 1: 3- Administration Health Condition 2: 8- Other Procedures Health Condition 3: M489- Spondylopathy, unspecified

Interventions

Intervention1: Lignocaine infusion: Intravenous Lignocaine infusion started at 2mg/kg/hour at start of induction of anaesthesia. Continued until closure of surgical site. Control Intervention1: Intrav

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged between 18 and 65 years of either sex,ASA I and ASA II undergoing general anesthesia for elective Robotic Spine surgery, Mallampati class I and II.

Exclusion criteria

Exclusion criteria: Patient refusal, Body mass index more than 35, Patients with cardiac, coronary, renal, hepatic, cerebral diseases and peripheral vascular diseases, Patients coming for emergency surgeries,Pregnancy,Neuromuscular disorder,Anticipated difficult intubation, Inability to use VAS (Visual Analogue Scale., History of allergy to Local Anaesthetics

Design outcomes

Primary

Measure	Time frame
Intraoperative hemodynamics postoperative Visual Analogue Scale(VAS) pain scores total analgesic consumptionTimepoint: Data will be collected over 3 months and analyzed at end of 3 months.	—

Secondary

Measure	Time frame
time to mobilization , hospital Length Of Stay(LOS), satisfaction scores and Quality of recovery scoresTimepoint: 3 months	—

Countries

India

Contacts

Public ContactDr Alia Vidyadhara

Manipal hospital , Bangalore

aliadr@gmail.com918095867447

Outcome results

None listed

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