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Timing of Withdrawal of the Laryngeal Mask Airway (LMA) in Children

NCT03105739 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 148

Last updated 2017-04-10

No results posted yet for this study

Summary

The purpose of this prospective, randomized study was to compare the incidence of adverse events associated with removal of the LMA either in deeply anesthetised or awake patients.

Conditions

  • Laryngeal Mask Airway Removal
  • Respiratory Complication

Interventions

OTHER

LMA removal

According to randomization, LMA device was removed at the end of surgery, either in deeply anesthetised patients or after consciousness recovery.

Sponsors & Collaborators

  • Hôpital d'enfants Béchir-Hamza

    lead OTHER

Principal Investigators

  • Sonia Ben Khalifa, PhD

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
1 Year
Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-10-05
Primary Completion
2017-03-29
Completion
2017-03-30

Countries

  • Tunisia

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03105739 on ClinicalTrials.gov