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Comparison of a drug given by topical spray and Intravenous route for surgeries done in throat - a clinical trial

Comparison of Lignocaine topical spray and Intravenous Lignocaine on total Propofol consumption to maintain Anesthesia during Suspension Laryngoscopy – A Randomized Clinical Trial. - nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/11/059415
Enrollment
60
Registered
2023-11-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

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 Spray 4%: 4ml of lignocaine 4% spray will be used before the procedure Control Intervention1: Lignocaine 2%: At dose of 1.5mg/kg given before induction of anesthesia through

Sponsors

Jawaharlal Institute of Postgraduate Medical Education and Research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients between 18-70 years of age planned for elective microlaryngeal surgery with suspension laryngoscopy 2)Patients with ASA physical status I and II

Exclusion criteria

Exclusion criteria: 1)Patients with a known hypersensitivity to Lidocaine 2)MLS done under LASER 3)Patients who were expected to have difficult intu-bation 4)Pregnant patients 5)Patients with known Arrhythmias 6)Patients with known Liver dysfunction 7)Uncontrolled hypertensive patients

Design outcomes

Primary

MeasureTime frame
To compare the mean propofol consumption required to maintain adequate depth of anaesthesia while using 4% Topical Lignocaine spray and 2% Intravenous Lignocaine during Suspension Laryngoscopy.Timepoint: end of surgery—

Secondary

MeasureTime frame
To compare the total additional dose of fentanyl used between the groupsTimepoint: at the end of surgery—

Countries

India

Contacts

Public ContactSwathi Bala G

Jawaharlal Institute of Postgraduate Medical Education and Research

anushacherian@gmail.com9789197801

Outcome results

None listed

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