To analyse the effectiveness of two different doses of nebulised dexmedetomidine in decreasing the hemodynamic response to laryngoscopy and endotracheal intubatio
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/11/059506
- Lead Sponsor
- Thamizhilakiya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1) patient Age between 18 and 60 years
2) ASA physical status 1 & 2
3) Normal airway belonging to both genders undergoing elective surgery under general anaesthesia with endotracheal intubation
Exclusion Criteria
1) predicted difficult airway
2) pregnancy, renal failure, uncontrolled hypertension, seizure disorder
3) patient on antidepressant/antipsychotic drugs
4) patient with poor cardiopulmonary reserve
5)BMI >35Kkg/m2
6) Dexmedetomidine allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the efficacy of two different doses of nebulised dexmedetomidine in decreasing hemodynamic response to laryngoscopy & endotracheal intubationTimepoint: 30mins before induction to 2hrs postoperatively
- Secondary Outcome Measures
Name Time Method To observe the effect of postoperative nausea & vomiting & sorethroatTimepoint: 2hrs postoperatively