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To evaluate the efficacy of two human airway devices - Baska mask and LMA Protector used for anesthetizing patients.

Phase 4
Conditions
Health Condition 1: D099- Carcinoma in situ, unspecified
Registration Number
CTRI/2024/05/066672
Lead Sponsor
Kalyan Singh Superspeciality cancer institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

18- 65 years

all patients Scheduled for elective surgery under general anaesthesia in supine position with expected duration of surgery less than 2 hours.

Exclusion Criteria

1.Upper airway anatomic variation or pathology.

2.Predicted difficult airway

3.High risk of aspiration (full stomach, gastroesophageal reflux, Pregnancy)

4.Body mass index greater than 30 kg/m2,

5.Patient refusal to participate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Oropharyngeal leak pressure during positive pressure ventilation. <br/ ><br> <br/ ><br>This outcome measure was used for sample size calculation.Timepoint: it will be assessed only once immediately after insertion and once successful ventilation is confirmed.
Secondary Outcome Measures
NameTimeMethod
1.First attempt success rate. <br/ ><br>2.Accuracy of size as per manufacturer recommendation. <br/ ><br>3.Insertion time. <br/ ><br>4.Ease of gastric tube placement. <br/ ><br>5.Anatomic position of device. <br/ ><br>6.Presence of blood & gastric contents on the device. <br/ ><br>7.Incidence & severity of postoperative sore throat at 1h, 4h & 24 h after surgery. <br/ ><br>8.Ease of insertion of SGAD. <br/ ><br>Timepoint: 1. Secondary outcome measures numbered 1-5,8 will be assessed immediately after insertion, only once. <br/ ><br>2.Secondary outcome measure number 6, will be assessed at the end of surgery. <br/ ><br>3. Secondary outcome measures number 7 will be assessed at 1h, 4h & 24 h after surgery. <br/ ><br>
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