Comparison of two upper airway devices with endotracheal tube in individuals undergoing laparoscopic surgeries
Not Applicable
Completed
- Conditions
- Health Condition 1: - Health Condition 2: -
- Registration Number
- CTRI/2019/01/016929
- Lead Sponsor
- Bhagat Phool Singh Government Medical College For Women
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 90
Inclusion Criteria
Patients who have the ability to give informed consent (i) Age: 18-65 years (ii) ASA Iâ??II (iii) elective surgery (iv) fasting for at least 8 hours.
Exclusion Criteria
Patients with ASA physical Status III or IV, anticipated difficult airway, mouth opening <2.5 cm, cervical spine disease ,obesity (body mass index > 35 kg/m 2 ), oropharyngeal pathology, emergency cases, cardiopulmonary disease, cervical spine fracture or instability, or at increased risk of aspiration (gastro-esophageal reflux disease, hiatus hernia, full stomach and heartburn), pregnant patients, reported history of any pathology of the neck or airway, history of lung diseases or oesophageal reflux will be excluded.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To determine the efficacy ease and insertion characteristics of supraglottic airway devices & endotracheal tubeTimepoint: 120 min
- Secondary Outcome Measures
Name Time Method To determine the hemodynamic changes and ventilation parameters and intraoperative and postoperative laryngo-pharyngeal morbidity and sealing pressureTimepoint: 24 hours