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Heart rate and blood pressure changes in opioid free anaesthesia and standard regimen

Comparison of haemodynamic responses to nasal intubation in patients receiving opioid free general anaesthesia using intravenous lignocaine versus standard regimen

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049938
Enrollment
20
Registered
2023-02-21
Start date
Unknown
Completion date
Unknown
Last updated
2023-03-06

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: Lignocaine 1.5mg/kg will be given as intravenous bolus before induction of anaesthesia followed by lignocaine 1mg/kg/hour intravenous infusion throughout the surgery Control

Sponsors

Amrita Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age 18-70 years, ASA physical status 1 to 2, Both males and females, Patients with head and neck malignancy undergoing major surgeries requiring nasal intubation

Exclusion criteria

Exclusion criteria: Basal heart rate Cardiac arrhythmias, Heart blocks, congestive heart failure, cardiogenic shock, Liver disorders with AST/ALT >2-3 times normal or renal diseases with eGFR Hypersensitivity to lidocaine or amide-type local anesthetic

Design outcomes

Primary

MeasureTime frame
Comparison of heart rate response (HR) at 1 min following nasal intubation with opioid free general anaesthesia using intravenous lignocaine versus standard regimen in patients undergoing major head and neck surgeries.Timepoint: 1 min following nasal intubation

Secondary

MeasureTime frame
Comparison of heart rate before induction, after induction, 3and 5min after intubation in opioid free general anaesthesia versus standard regimen. Systolic, Diastolic and Mean arterial pressure (MAP) at the same time points, time required to intubate and number of attempts at intubation will also be compared.Timepoint: before induction, after induction, 3and 5min after intubation

Countries

India

Contacts

Public ContactDr Sunil Rajan

Professsor in Anaesthesia, Amrita Institute of Medical Sciences, Kochi

sunilrajan@aims.amrita.edu9447464652

Outcome results

None listed

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