Study to know the effect of two drugs after removing endotracheal tube.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/03/050769
- Lead Sponsor
- DR UMESH N P
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patient willing to give informed consent.
2.Age between 18-65 years of either gender.
3.American Society of Anaesthesiologist (ASA) grade I and II.
4.Modified Mallampatti grade I-II
5.Patients undergoing elective surgical procedures of duration 90 to 120 minutes under general anesthesia with endotracheal intubation.
Exclusion Criteria
1.Patients undergoing emergency surgeries.
2.Procedures requiring perioperative nasogastric tube placement.
3.Patients with a high risk of aspiration.
4.Anticipated difficult airway
5.Pregnant women.
â??Active upper respiratory tract infections.
â??Preoperative sore throat.
â??Previous history of Gastroesophageal reflux disease (GERD).
â??Head and neck surgeries and surgeries requiring prone position.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method TO DETERMINE THE EFFICACY OF INTRACUFF DEXAMETHASONE (8 MG ) WHEN COMPARED TO 2% LIGNOCAINE ON POST EXTUBATION RESPONSE IN PATIENTS UNDERGOING ELECTIVE SURGERIESTimepoint: 2hrs, 6hrs, 12hrs and 24hrs
- Secondary Outcome Measures
Name Time Method to compare severity of post operative sore throat and hoarse ness of voiceTimepoint: 2 hours, 6 hours, 12 hours, 24 hours