a comparison of success rate of blind endotracheal intubation through i-gel and ambu auragain in adult.
Phase 3
- Conditions
- Health Condition 1: T758- Other specified effects of external causesHealth Condition 2: T07- Unspecified multiple injuries
- Registration Number
- CTRI/2023/10/059006
- Lead Sponsor
- maharaja agrasen medical college
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
BELONGING TO ASA PHYSICAL STATUS I OR II.
Exclusion Criteria
Patients with pregnancy, known or
predicted difficult airway, reduced lung
compliance, inter incisor gap < 3.0cm, BMI
>35 kg/m2
, High risk for pulmonary aspiration
(non fasted, gastroesophageal reflux disease).
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare success rate of blind endotracheal intubation through i-gelTM & Ambu AuraGain.Timepoint: 48weeks
- Secondary Outcome Measures
Name Time Method 1. To compare success rate of device [SAD] insertion [Number of insertion attempts, time of <br/ ><br>insertion]. <br/ ><br>2. Postoperative complications. <br/ ><br> Blood on device. <br/ ><br> Sore throat. <br/ ><br> Hoarseness of voice. <br/ ><br> DysphagiaTimepoint: 2 YEARS