Simpler and less invasive device to give general anesthesia to children undergoing laparoscopic surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Children scheduled for routine elective laparoscopic surgeries
- Registration Number
- CTRI/2017/05/008470
- Lead Sponsor
- Army Hospital Research Referral New Delhi India
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
All patients scheduled for elective laparoscopic surgery in a tertiary care pediatric surgery center and their parents consenting for their children to participate in the study protocol will be included in the study.
ASA I-II
BMI 20-30 kg/m2
Exclusion Criteria
Respiratory tract infection
Inadequate fasting as per standard fasting guidelines
Difficult airway
Emergency surgery
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Oro-pharyngeal seal pressure (OSP) of the supraglottic deviceTimepoint: 2 min after insertion, <br/ ><br>10 min after creation of pneumoperitoneum, <br/ ><br>every 30 min thereafter till the end of surgery
- Secondary Outcome Measures
Name Time Method heart rate, non-invasive blood pressure, SpO2, ECG, Peak airway pressure, respiratory rate, tidal volume will be continuously monitored and notedTimepoint: every 30 min from the start of anesthesia;sore throat, hoarseness of voice, oral bleedingTimepoint: At extubation <br/ ><br>2 h after extubation <br/ ><br>6 h after extubation