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COMPARISON OF LIGNOCAINE 2% JELLY AND STERILE WATER-BASED LUBRICANT TO REDUCE POSTOPERATIVE SORE THROAT

Not Applicable
Conditions
Health Condition 1: J958- Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified
Registration Number
CTRI/2024/05/067584
Lead Sponsor
K S Hegde Medical Academy
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Patient belonging to 18-65 years of age undergoing elective surgeries under GA

requiring orotracheal intubation.

American Society of Anaesthesiologists (ASA) grade I, II and III

Exclusion Criteria

Patient with difficult airway, More than one attempt of intubation, Head and neck surgery, Prolonged surgery more than 4 hours, Pre-existing respiratory complications, Patient refusal

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate the occurrence of postoperative sore throat after the application of lignocaine 2% <br/ ><br>jelly versus sterile water-based lubricant (K-Y <br/ ><br>® jelly). <br/ ><br>Timepoint: 1st hour , 4th hour and 24th hour in the postoperative period
Secondary Outcome Measures
NameTimeMethod
To assess the incidence of postoperative cough and hoarseness in the patient after the <br/ ><br>application of lignocaine 2% jelly and sterile water-based lubricant (K-Y <br/ ><br>® jelly). <br/ ><br>Timepoint: 1, 4 and 24 hrs in the postoperative period
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