TO DETERMINE THE CHANGE IN THE PRESSURE OF CUFF OF A ADAPTIVE CUFF ENDOTRACHEAL TUBE IN PATIENTS WHO UNDERGO SURGERY UNDER GENERAL ANESTHESIA
Not Applicable
- Conditions
- Health Condition 1: 4- Measurement and MonitoringHealth Condition 2: 4- Measurement and Monitoring
- Registration Number
- CTRI/2022/10/046388
- Lead Sponsor
- PTBDSHARMA POST GRADUATE INSTITUTE OF MEDICAL SCIENCESROHTAK
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Adult patients, aged 16-60 years ASA 1-3 planned for surgery expected to last a minimum of one hour or more under general anesthesia with airway secured with an endotracheal tube.
Exclusion Criteria
Patients who refuse to give consent, with risk of aspiration, with an anticipated difficult airway, with known cardiovascular disease shall be excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess variation in cuff pressure in adaptive cuff endotracheal tube under controlled ventilation in adult patientsTimepoint: 5 MIN,10MIN,15MIN,20 MIN,30 MIN,60MIN AFTER THE INDUCTION OF ANESTHESIA
- Secondary Outcome Measures
Name Time Method Difficulty /complication while using adaptive cuff endotracheal tubeTimepoint: FROM INDUCTION TO REVERSAL OF ANESTHESIA;Minimum cuff pressure for ventilation without producing leakTimepoint: NOT APPLICABLE;To assess the highest cuff pressure reached with change in the ventilatory phase <br/ ><br> <br/ ><br>Timepoint: 5 MIN,10MIN,15MIN,20 MIN,30 MIN,60MIN AFTER THE INDUCTION OF ANESTHESIA