CTRI/2023/11/060084Not yet recruitingPhase 1
Comparison of endtidal sevoflurane concentration required for optimal depth of anaesthesia during opioid free general anesthesia using intravenous lignocaine versus standard care. - nil
Trial Snapshot
- Phase
- Phase 1
- Status
- Not yet recruiting
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •American Society of Anesthesiologists physical status (ASA PS) 2 to 3,
- •Carcinoma tongue and alveolus undergoing tumor resection surgeries requiring nasal intubation
Exclusion Criteria
- •i.Patients with basal HR <60/min,
- •ii.on beta blockers,
- •iii.having cardiac arrhythmias, heart blocks, congestive heart failure,
- •iv.liver disorders with aspartate aminotransferase /alanine transaminase >2-3 times normal
- •v.renal diseases with estimated glomerular filtration rate <60ml/min/1.73m2
- •vi.hypersensitivity to lignocaine
- •vii.awake fiberoptic bronchoscope assisted intubation,
- •viii.carcinoma maxilla, craniofacial resection, exenteration, scalp, mastoid and surgeries requiring neuro assistance
- •ix.supplemental regional anaesthesia.
Investigators
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