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Laryngeal Mask Airway Versus Air Q Laryngeal Airway

Laryngeal Mask Airway Versus Air Q Laryngeal Airway in Dacryocystorhinostomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04021407
Enrollment
72
Registered
2019-07-16
Start date
2018-04-01
Completion date
2019-06-01
Last updated
2019-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Airway Devices

Keywords

AirQ, LMA, dacrocystorhinostomy surgery

Brief summary

Nowadays, supraglottic airway devices are simple and effective alternatives to endotracheal intubation. Both laryngeal mask airway LMA and air-Q airway are supraglottic airway devices that can be used to maintain and protect airways from aspiration of secretions and blood during DCR surgery. The present study was designed to compare standard LMA versus air Q as regards the sealing effect and aspiration of blood in DCR surgery.

Detailed description

72 patients were divided into two groups, 36 patients each, named LMA group, and air Q group according to supraglottic devices used. The following parameters were recorded in both studied groups, continuous Electrocardiography (ECG), heart rate (HR), means arterial pressure (MAP), arterial oxygen saturation (SpO2), end tidal carbon di-oxide (PCO2)..Oro pharyngeal leak pressure in (cmH2O), exhaled tidal volume in (ml), leak volume in (ml), leak fraction in (%) number of shifting from LMA to air Q or ETT and shifting from air Q to LMA or ETT was recorded with absence or presence of surgical blood on The undersurface of the device used.

Interventions

DEVICELMA group

patients were ventilated with LMA

DEVICEAirQ group

patients were ventilated with AirQ airway

Sponsors

Menoufia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Participiant Investigator

Intervention model description

Parallel assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Both sex * Age: 18-60 years * ASA I-II * Patients scheduled for dacryocystorhinostomy surgery

Exclusion criteria

* Any pathology of the neck, upper respiratory tract, upper alimentary tract * Patients with a history of gastric regurgitation, heartburn * Morbid obese, * Patients with esophageal reflux (hiatus hernia) * Anticipating difficult airway management * Patients with coagulation disorders

Design outcomes

Primary

MeasureTime frameDescription
Oro pharyngeal leak pressure in (cmH2O)Just after insertion of supraglottic airway devicesBy setting the pop-off valve to limit peak airway pressure to 40 cm H2O and allowing airway pressure to increase at a fresh gas flow of 3 L/min until audible noise was heard over the mouth and no further increase in airway pressure is observed.

Secondary

MeasureTime frameDescription
Leak fraction in (%)Just after insertion of supraglottic airway devicesLeak fraction in (%)( Leak was calculated by subtracting the expiratory volume from the inspiratory volume and expressed as a fraction of the inspiratory volume). were evaluated just before surgery

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026