A Randomised Controlled Trial to Evaluate and Compare the Air-q Intubating Laryngeal Airway with Cuffed Endotracheal Tube during Pressure Controlled Ventilatio
Not Applicable
Completed
- Conditions
- Health Condition 1: null- ASA PHYSICAL STATUS 1 AND 2Health Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2021/03/031997
- Lead Sponsor
- Maulana Azad Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1. ASA Grade 1 or 2
2. BMI 18-30 kg/square metres
3. Anticipated duration of surgery not exceeding 2 hours
Exclusion Criteria
1. known or predicted difficult airway.
2. acute or chronic lung disease.
3. Inadequate cervical mobility/ cervical malformation.
4. Pregnancy.
5. Surgeries of head and neck.
6. Procedures not performed in the supine position.
7. Laparoscopic surgeries.
8. Full stomach/ increased risk of aspiration ( GERD, diabetes mellitus, hiatus hernia)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Difference in leak fractions between the two airway devices.Timepoint: after insertion and 30 minutes after initial set of readings.
- Secondary Outcome Measures
Name Time Method airway leak pressuresTimepoint: after insertion of device;difference in leak volumesTimepoint: after insertion and 30 minutes after initial set of readings;hemodynamic response to device insertion: Heart rate, blood pressure (SBP, DBP and Mean BP)Timepoint: at insertion;insertion characteristics- time, ease, attempts and assisting maneuversTimepoint: at insertion;Morbidity due to device- Blood staining, hoarseness, dysphagia, sore throatTimepoint: after removal of device