To see effect of LMA proseal and LMA protector on heart rate and blood pressure after removing endotracheal tube and putting LMA in adult patient coming out of general anaesthesia after surgery
Phase 4
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/049716
- Lead Sponsor
- Department of Anaesthesia and Intensive Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
1. Age group of 18 to 60 years
2. ASA (American Society of Anaesthesiologists) status I and II
3. Patients undergoing elective surgery requiring general anaesthesia with endotracheal intubation.
Exclusion Criteria
1. Patients with difficult airway with Airway difficulty score >8
2. Morbid obesity BMI > 35 kg/m2
3. Known airway pathology
4. Oropharyngeal surgeries
5. Surgery more than 3 hours
6. Patients at increased risk of aspiration like gastroesophageal reflux, peptic ulcer
7. Previous upper gastrointestinal surgery
8. Known or anticipated difficult tracheal intubation or facemask ventilation
9. Coagulopathy or history of anticoagulant use
10. Cardio respiratory or cerebrovascular disease
11. Cervical spine injury
12. Pregnant Patients
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the hemodynamic responses during extubation using Baileys maneuver with Laryngeal Mask Airway Protector or Proseal LMATimepoint: Hemodynamic response would be noted After SAD insertion,after remoal of ETT,1,2,3,5and 10 min afterward and then at SAD removal and 1,2,3,5 and 10 min afterward
- Secondary Outcome Measures
Name Time Method 1) To compare secondary parameters such as cough reflex awakening after extubation using Baileys maneuver with Laryngeal Mask Airway Protector device or Proseal LMA. <br/ ><br> 2) To observe any adverse effects such as bleeding, trauma or sore throat, if any.Timepoint: Adverse effect if any, will be noted in postoperative room till first 24 hours post operatively (Once in post operative room and once after 24 hours of removal of SAD).