To compare the incidence of any respiratory events after total intravenous anaesthesia with Propofol and inhalational anaesthesia with Sevoflurane following removal of proseal laryngeal mask airway
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/07/055369
- Lead Sponsor
- Maulana Azad Medical College And Associated Lok Nayak Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.6months to 7years of age scheduled to undergo elective lower limb,lower abdominal and genitourinary surgeries
2.American Society of Anaesthesiologists Grade I and II
3.Patients in whom the anticipated duration of surgery <2 hours
Exclusion Criteria
1.Recent [ <2weeks] upper respiratory tract infection, acute exacerbation of Asthma , chronic respiratory disease
2.Congenital heart disease
3.Neurological disorder
4.Hiatal hernia
5.Known or predicted difficult airway
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of any respiratory event [cough, biting on the airway device/teeth clenching,oxygen desaturation,breath holding,laryngospasm,bronchospasm or upper airway obstruction] during removal of Proseal laryngeal mask airway & emergence from anaesthesia.Timepoint: 2 hours
- Secondary Outcome Measures
Name Time Method 1.Prevalence of individual respiratory events. <br/ ><br>2.Airway hyperreactivity score. <br/ ><br>3.Emergence time. <br/ ><br>4.Incidence of emergence agitation using a 4 point scale. <br/ ><br>5.Duration of post anaesthetic care unit stay. <br/ ><br>6.Post operative nausea & vomiting. <br/ ><br>7.Hemodynamic parameters (systolic blood pressure,diastolic blood pressure,heart rate,oxygen saturation)during emergence. <br/ ><br>Timepoint: 24 hours