Desflurane in Children With Laryngeal Mask Airway

NCT ID: NCT02470442

Last Updated: 2017-08-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-06-30

Study Completion Date

2016-03-31

Brief Summary

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The purpose of this study is to characterize the airway responses to desflurane during maintenance of and emergence from anesthesia in children whose airways were supported with laryngeal mask airways (LMAs).

Detailed Description

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Conditions

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Desflurane Anesthesia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Sevoflurane/Desflurane

After induction of general anesthesia with sevoflurane, anesthesia was maintained with desflurane.

Group Type EXPERIMENTAL

Sevoflurane/Desflurane

Intervention Type DRUG

Anesthesia induced with sevoflurane and anesthetic maintenance with desflurane

Sevoflurane

the anesthetic induction and maintenance with sevoflurane.

Group Type EXPERIMENTAL

Sevoflurane

Intervention Type DRUG

Anesthesia induced with sevoflurane and anesthetic maintenance with sevoflurane

Interventions

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Sevoflurane/Desflurane

Anesthesia induced with sevoflurane and anesthetic maintenance with desflurane

Intervention Type DRUG

Sevoflurane

Anesthesia induced with sevoflurane and anesthetic maintenance with sevoflurane

Intervention Type DRUG

Other Intervention Names

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suprane

Eligibility Criteria

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Inclusion Criteria

* scheduled for elective surgery under general anesthesia with laryngeal mask airway

Exclusion Criteria

* history of reactive airways disease with an acute exacerbation within the past 2 weeks
* if wheezing or an active upper respiratory infection was present on the day of surgery
* if there was a history of malignant hyperthermia
* a history of moderate-to-severe hepatic dysfunction following anesthesia with desflurane not otherwise explained.
Minimum Eligible Age

2 Years

Maximum Eligible Age

6 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Seoul National University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Jin-Tae Kim

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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JinTae Kim, MD. PhD.

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Hospital

Locations

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Seoul national university hospital

Seoul, , South Korea

Site Status

Countries

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South Korea

Other Identifiers

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H-1504-116-668

Identifier Type: -

Identifier Source: org_study_id

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