To study the effects of dexmedetomidine during extubation when given intranasally
Not Applicable
- Registration Number
- CTRI/2024/07/071105
- Lead Sponsor
- MS Ramaiah Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age between 18 and 60 years old of either gender.
American society of Anaesthesiologists physical status (ASA) 1 and 2
Exclusion Criteria
Refusal to consent for surgery
Pregnant and lactating mother
Severe cardiovascular, renal or hepatic disorders
Patients with nasal polyps or nasal ulcers
Patients with allergy to the drug
Patients with anticipated difficult airway
Patients undergoing surgeries in prone position
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method incidence and severity of cough grade during extubationTimepoint: Immediately after extubation <br/ ><br>
- Secondary Outcome Measures
Name Time Method Comparison of hemodynamic parameters, extubation time and sedation score with control groupTimepoint: Hemodynamic parameters will be recorded at 4 points, before intubation, 5minutes after giving intranasal dexmedetomidine, immediately before extubation and 5 min after extubation <br/ ><br>Sedation will be measured with Ramsay Sedation Scale