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Study to compare the requirement of analgesic in patients scheduled to undergo robotic assisted spine surgery , by giving one group of patients local anaesthetic infusion and the other group saline infusion(placebo).

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077208
Enrollment
128
Registered
2024-11-21
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: O- Medical and Surgical

Interventions

Intervention1: Lignocaine infusion: Intravenous Lignocaine is given as an infusion intraoperatively at a specified rate of 2mg/kg/hour in one group. This infusion is started at induction of anaesthesi

Sponsors

Manipal Hospital Bangalore
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult patients aged between 18 and 65 years of either sex. 2. ASA I and ASA II undergoing general anesthesia for elective Robotic Spine surgery. 3. Mallampati class I and II

Exclusion criteria

Exclusion criteria: 1. Patient refusal. 2. Body mass index >= 35 kg/ m2 3. Patients with cardiac, coronary, renal, hepatic, cerebral diseases and peripheral vascular diseases. 4. Patients coming for emergency surgeries. 5. Pregnancy. 6. Neuromuscular disorder. 7. Anticipated difficult intubation. 8. Inability to use VAS (Visual Analogue Scale). 9. History of allergy to Local Anaesthetics

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale score ranging from 0 to 10 (0 no pain, 10 worst imaginable pain) to score the postoperative pain.Timepoint: The VAS scores will be recorded immediately in the recovery room at 30 minutes, 2 hr,4hr, 8hr, 12hr , and 24 hours postoperatively during bed rest and at 8, 12, and 24 hours during movement.

Secondary

MeasureTime frame
Total analgesic used between both groups Total propofol used Richmond agitation sedation scale Length of hospital stay time to mobilisation , first oral feed Quality of recovery score Satisfaction scoreTimepoint: from immediate post operatively upto 1 month

Countries

India

Contacts

Public ContactAnjana Kashyap

Manipal hospital, Bangalore

visitanju26@gmail.com919620436462

Outcome results

None listed

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