Comparison of lidocaine lozenges and lidocaine nebulization for providing better condition during fiberoptic intubatio
Not Applicable
- Conditions
- Health Condition 1: 8- Other Procedures
- Registration Number
- CTRI/2022/09/045699
- Lead Sponsor
- OK NAYAK HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
American Society of Anaesthesiologist physical status classes (ASA) I & II patients age between 18 and 70 years of either sex scheduled for elective surgery under general anaesthesia with anticipated difficult airway requiring awake nasal/oral fiberoptic intubation
Exclusion Criteria
1.Uncooperative patients
2.Pregnant patients
3.Known Allergy to lidocaine
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time taken for successful awake fiberoptic guided intubationTimepoint: defined as time taken from insertion of fiberoptic guided intubation inside nostril/ mouth to square shaped capnograph
- Secondary Outcome Measures
Name Time Method 1.First attempt success rate. <br/ ><br>2.Anaesthesiologist satisfaction (Ease of procedure, level of gag reflex, ease of application of anesthetic agent). <br/ ><br>3.Hemodynamic variable (heart rate and mean arterial pressure) will be recorded at baseline, 1min, 3min and 5min after the procedure. <br/ ><br>4.Patients satisfaction (Tolerability of procedure, aversive symptoms experienced during and/or after procedure, patient�s preference for repetition of procedure). <br/ ><br>5.Any signs of lignocaine toxicity such as ECG changes, seizures, and bronchoconstriction if any.Timepoint: from starting of the awake fiberoptic intubation till 5 min of the procedure