A clinical trial to compare the effectiveness of two devices, The Baska mask and The Laryngeal mask airway supreme used to provide breath while giving anesthesia to the patient
Not Applicable
Completed
- Registration Number
- CTRI/2017/08/009255
- Lead Sponsor
- Sreedevi J
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
1.Patients with informed consent
2.ASA 1 and ASA 2
3.Body Mass Index <30
4.18 - 60 years
5.Short surgeries lasting less than one hour
Exclusion Criteria
1.Patients refusal or inability to give informed consent
2.Patients with neck pathology
3.Previous or anticipated problem with upper airway or upper gastro intestinal tract
4.Pregnancy
5.Patients at increased risk of aspiration
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.rate of first time successful placement of the supraglottic device, <br/ ><br>2.the seal pressure created by the supraglottic device.Timepoint: 5 seconds after inserting the device
- Secondary Outcome Measures
Name Time Method laryngopharyngeal morbidityTimepoint: sore throat, hoarseness and dysphagia in the post operative recovery room and 24 hours post surgery[