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Clinical Trials/CTRI/2024/08/071934
CTRI/2024/08/071934Not yet recruitingPhase 3

Comparison of Nitro-glycerine spray and Lignocaine spray for attenuating the pressor response during laryngoscopy and endotracheal intubation in patients undergoing elective surgery under general anaesthesia

Peoples Hospital1 site in 1 country120 target enrollmentStarted: August 14, 2024Last updated:

Trial Snapshot

Phase
Phase 3
Status
Not yet recruiting
Enrollment
120
Locations
1
Primary Endpoint
Attenuation of pressor response

Study Overview

Brief Summary

This is a postgraduate thesis to study the attenuation response of nitroglycerine spray and 10% lignocaine spray. This study comprises of 120 patients divided into 2 groups. One group will recieve Nitroglycerine spray and the other will receive lignocaine spray prior to laryngoscopy. The stress response during laryngoscopy will be recorded for 10 minutes and compared.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Investigator Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Asa grade 1 and 2 Elective surgery under general anaesthesia with endotracheal intubation.

Exclusion Criteria

  • Lack of patients consent Age less than 18 years and more than 60 years ASA grade 3 and more Patient with anticipated difficult airway Patient with hypersensitivity to any of the drugs used Pregnant and lactating mothers Hypertensive patients.

Outcomes

Primary Outcomes

Attenuation of pressor response

Time Frame: 10 minutes

Secondary Outcomes

  • Hemodynamic parameters(10 minutes)

Investigators

Sponsor Class
Private medical college
Responsible Party
Principal Investigator
Principal Investigator

Dr Pushpraj Brahme

Peoples College of Medical Sciences and Research Centre

Study Sites (1)

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