Randomized comparison to study effect of lignocaine infusion as a part of analgesic regimen in Robotic lumbar spine surgery
Phase 2
- Conditions
- Health Condition 1: 3- AdministrationHealth Condition 2: 8- Other ProceduresHealth Condition 3: M489- Spondylopathy, unspecified
- Registration Number
- CTRI/2024/02/062900
- Lead Sponsor
- ONE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intraoperative hemodynamics <br/ ><br>postoperative Visual Analogue Scale(VAS) pain scores <br/ ><br>total analgesic consumptionTimepoint: Data will be collected over 3 months and analyzed at end of 3 months.
- Secondary Outcome Measures
Name Time Method time to mobilization , hospital Length Of Stay(LOS), satisfaction scores and Quality of recovery scoresTimepoint: 3 months