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Use of Laryngeal Mask Airway in Pediatric Adenotonsillectomy

Virginia Commonwealth University (VCU) logo

Virginia Commonwealth University (VCU)

Status

Completed

Conditions

Laryngeal Mask Airway
Tonsillectomy

Treatments

Device: Endotracheal Tube
Device: Laryngeal mask airway

Study type

Interventional

Funder types

Other

Identifiers

NCT01141660
HM10692

Details and patient eligibility

About

The aim of the current study is to compare the use of laryngeal mask airway (LMA) and endotracheal tube (ETT) in pediatric adenotonsillectomy. The primary objective is to assess the incidence of post-operative laryngospasm between the LMA and ETT. The investigators also sought to compare anesthetic, operative, and recovery times in the LMA and ETT groups. We hypothesized that the LMA would be a safe efficient alternative to the ETT.

Enrollment

131 patients

Sex

All

Ages

2 to 12 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children 2 to 12 years of age undergoing elective adenotonsillectomy for obstructive sleep apnea or chronic tonsillitis were included in the study.

Exclusion criteria

  • Exclusion criteria were as follows: Body Mass Index (BMI) greater than 35 and craniofacial anomalies.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

131 participants in 2 patient groups

Endotracheal Tube
Experimental group
Description:
Children undergoing adenotonsillectomy are randomized to endotracheal tube or laryngeal mask airway.
Treatment:
Device: Endotracheal Tube
Laryngeal Mask Airway
Experimental group
Description:
Children undergoing adenotonsillectomy are randomized to endotracheal tube or laryngeal mask airway.
Treatment:
Device: Laryngeal mask airway

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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