Comparative study to see the gastric volume in two airway device groups
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/07/044102
- Lead Sponsor
- AIIMS rishikesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age >= 18 years and <= 65 years.
2.BMI<=30 kg/m2
3.American Society of Anesthesiologists (ASA) grading I-II.
4.Posted electively for laparoscopic lower abdominal procedures
Exclusion Criteria
1.Preoperative sore throat and/or hoarseness.
2.Known risk of gastric aspiration.
3.Mallam Pati grade 3 or 4.
4.Facial and upper airway abnormalities that make mask ventilation and tracheal intubation difficult.
5.Hiatus hernia.
6.Pregnant and breastfeeding females.
7.Anticipated difficult intubation
8.Full stomach
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Antral cross-sectional area, as measured by ultrasoundTimepoint: time points(baseline, Immediately after induction, at 1 hour, at the end of surgery and 1 hour post surgery)
- Secondary Outcome Measures
Name Time Method Vital parameters (Heart Rate, Systolic Blood Pressure, Diastolic BP, MAP, SpO2, ETCO2)and intra abdominal pressure <br/ ><br>Ventilation parameters (TV, Leak Fraction, Leak Volume, Peak pressure, plateau pressure) <br/ ><br>Time (in hour minutes) to tolerance of clear fluids <br/ ><br>Time(in hour minutes) to tolerance of Light diet <br/ ><br>Time (in hour minutes) to achieve first bowel movement or first flatus, whichever is earlier <br/ ><br>Length of stay and days to discharge in patients <br/ ><br>Timepoint: time points(baseline, Immediately after induction, at 1 hour, at the end of surgery and 1 hour post surgery)