Dose Titration of Propofol for Tracheal Intubation in Children With Sevoflurane Inhalation Induction
NCT ID: NCT01084031
Last Updated: 2014-02-19
Study Results
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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COMPLETED
NA
50 participants
INTERVENTIONAL
2009-11-30
2011-03-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
SINGLE_GROUP
SUPPORTIVE_CARE
DOUBLE
Study Groups
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propofol
propofol
intravenous propofol with sevoflurane inhalation induction
Interventions
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propofol
intravenous propofol with sevoflurane inhalation induction
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Evidence of cardiorespiratory disease
* Those who were obese or allergic to any of the anesthetic agents in this study
* Those with an anticipated difficult airway, full stomach
* History of malignant hyperthermia or other myopathy were excluded.
6 Months
5 Years
ALL
No
Sponsors
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Yonsei University
OTHER
Responsible Party
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Principal Investigators
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Hae Keum Kil
Role: PRINCIPAL_INVESTIGATOR
Department of Anesthesiology and Pain Medicine, Yonsei University College of Medicine, Seoul, Korea
Other Identifiers
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4-2009-0470
Identifier Type: -
Identifier Source: org_study_id
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