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The Comparison of Two Different Methods of Partial Inflation of Cuff for Facile Insertion of Laryngeal Mask Airway in Pediatric Patients

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Yonsei University

Status

Completed

Conditions

Surgical Complications From General Anesthesia

Treatments

Device: The cuff inflation by the resting volume
Device: The cuff inflation by the maximum volume

Study type

Interventional

Funder types

Other

Identifiers

NCT01435239
1-2011-0046

Details and patient eligibility

About

Partial cuff inflation before insertion is generally used for laryngeal mask airway insertion in children. However, it is not proven how much the cuff should be inflated. The aim of this study is to compare efficacy between the method using the resting volume and the method using half the maximum volume for partial cuff inflation.

Enrollment

78 patients

Sex

All

Ages

Under 9 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • children (0-9 years of age)
  • children who is scheduled for elective surgery of short duration (less than 2 hr) undergoing general anesthesia using LMA-classic

Exclusion criteria

  • patients with an abnormal airway
  • patients with reactive airway disease
  • patients with gastroesophageal reflux disease
  • patients with chronic respiratory disease
  • patients who has a history of an upper respiratory tract infection in the preceding 6-week period

Trial design

78 participants in 2 patient groups

resting volume group
Experimental group
Treatment:
Device: The cuff inflation by the resting volume
maximum volume group
Active Comparator group
Treatment:
Device: The cuff inflation by the maximum volume

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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