About this trial
Video laryngeal masks (VLMAs) are increasingly used as a minimally invasive alternative in airway management. The use of neuromuscular blocking agents can affect VLMA placement and airway physiology. As a result, there may be differences in postoperative respiratory complications and middle ear pressure.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Cases lasting longer than 1 hour
Participants with body mass index >30
Participants with ASA I, II, III
Disqualifiers
Participants with a body mass index < 30
Pregnant women
Participants with expected difficult airway passage
Cases lasting less than 1 hour
Trial population
Participants who will use a laryngeal mask in their surgical procedures
Trial design
Cohort
Prospective
Treatments tested in this trial
using rocuronium before vide laryngeal mask airway
Drugusing rocuronium before video laryngeal mask airway
Treatment groups
Trial outcomes
Primary outcomes
Postoperative sore throat
Postoperative sore throat will be assessed using NRS (0: no pain, 10: most severe pain).
Secondary outcomes
Changes in middle ear pressure
In this study, middle ear pressure will be assessed using tympanometry during the preoperative period, immediately after induction of anesthesia, following endotracheal intubation, and at the 3rd and 5th minutes thereafter.
Oropharyngeal leak pressure
Oropharyngeal leak pressure (OLP) was measured by closing the adjustable pressure-limiting (APL) valve with a fresh gas flow of 3 L/min, and the airway pressure at which an audible leak occurred or the manometer pressure reached a plateau was recorded as the OLP (cmH₂O).
video laryngeal mask airway placement time
Video laryngeal mask airway placement time will be recorded after induction.
Sponsors and contacts
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