Comparison of a drug given by topical spray and Intravenous route for surgeries done in throat - a clinical trial
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
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
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
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method To compare the total additional dose of fentanyl used between the groupsTimepoint: at the end of surgery