The Effects of GMA-TULIP, I-gel, and BlockBuster Laryngeal Mask in Surgeries With Lateral Position Under General Anesthesia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorThe Second Affiliated Hospital of Chongqing Medical University

About this trial

To compare the efficacy and safety of traditional inflatable laryngeal mask, i-gel non-inflatable laryngeal mask and GMA-TULIP non-inflatable laryngeal mask in surgeries with lateral position under general anesthesia, so that providing evidence for the selection of laryngeal mask in surgeries with lateral position.

Eligibility criteria

Qualifiers

Patients received surgeries in lateral position with an estimated surgery duration of less than 3 hours under general anesthesia.

Ages between 18 to 80, and body mass index less than 28 kg/m².

American Society of Anesthesiologists (ASA) Grades I-III.

Patients are willing to participate and be able to understand and sign an informed consent form.

Disqualifiers

Individuals with an open bite of less than 2cm.

Individuals with a history of obvious regurgitation of gastric contents and risk factors for aspiration.

Patients with combined pharyngeal and laryngeal lesions.

Predicting difficult airway patients.

Trial design

Treatments tested in this trial

  • GMA-TULIP Laryngeal Mask
  • i-gel Laryngeal Mask
  • BlockBuster Laryngeal Mask

Treatment groups

102 Participants
are divided into 3 treatment groups