CTRI/2026/01/101397Not yet recruitingPhase 2/3
A prospective randomised study comparing the clinical performance of Proseal LMA and Baska Mask in adult patients undergoing elective surgery under general anaesthesia with controlled ventilation.
Department of Anaesthesia1 site in 1 country80 target enrollmentStarted: January 21, 2026Last updated:
Trial Snapshot
- Phase
- Phase 2/3
- Status
- Not yet recruiting
- Sponsor
- Department of Anaesthesia
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- To compare the clinical performance of both the LMA
Study Overview
Brief Summary
This study is a prospective randomised study comparing the clinical efficacy of the Proseal LMA and Baska mask in adult patients undergoing elective surgeries in general anaesthesia with controlled ventilation.
we will be assessing number of attempts taken for successful insertion, oropharyngeal seal pressure, ease of insertion of device, hemodynamic parameters, and complications if any.
Study Design
- Study Type
- Interventional
- Allocation
- Other
- Masking
- Participant and Investigator Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 60.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •ASA Grade 1 and 2 undergoing elective surgery in supine position under general anaesthesia.
Exclusion Criteria
- •ASA Grade3/4 pregant patient surgery duration more than 4 hours.
Outcomes
Primary Outcomes
To compare the clinical performance of both the LMA
Time Frame: postoperatively complications to be assessed for 24 hours if any
Secondary Outcomes
- number of attempts for successful insertion of device(patients to be assessed for 24 hours postoperatively)
- orophayngeal seal pressure(patients to be assessed for 24 hours postoperatively)
- complications if any(patients to be assessed for 24 hours postoperatively)
Investigators
Monika
LLRM Medical College
Study Sites (1)
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