Dexmedetomidine Versus Sevoflurane in Children With Anticipated Difficult Intubation
NCT ID: NCT04426552
Last Updated: 2020-06-12
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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UNKNOWN
PHASE2
40 participants
INTERVENTIONAL
2020-06-01
2020-10-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
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Dexmedetomidine
have a bolus of dexmedetomidine one μg/kg (Precedex; Hospira, Inc, Lake Forest, IL) administered for 10 minutes, followed by a continuous infusion at 0.7 μg • kg-1 • h-1 during FOI
dexmedetomidine
will have a bolus of dexmedetomidine one μg/kg (Precedex; Hospira, Inc, Lake Forest, IL) administered for 10 minutes, followed by a continuous infusion at 0.7 μg • kg-1 • h-1 during FOI
Sevoflurane
(sevoflurane) will be preoxygenated using face mask with 100% oxygen for 3 min to increase oxygen reserve and then inhalational induction will be started with sevoflurane in 100% oxygen using Ayre's piece circuit/MapelsonD circuit according to age and weight of the patient while performing fiberoptic intubation
sevoflurane
preoxygenated using face mask with 100% oxygen for 3 min to increase oxygen reserve and then inhalational induction will be started with sevoflurane in 100% oxygen using Ayre's piece circuit/MapelsonD circuit according to age and weight of the patient while performing fiberoptic intubation
Interventions
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dexmedetomidine
will have a bolus of dexmedetomidine one μg/kg (Precedex; Hospira, Inc, Lake Forest, IL) administered for 10 minutes, followed by a continuous infusion at 0.7 μg • kg-1 • h-1 during FOI
sevoflurane
preoxygenated using face mask with 100% oxygen for 3 min to increase oxygen reserve and then inhalational induction will be started with sevoflurane in 100% oxygen using Ayre's piece circuit/MapelsonD circuit according to age and weight of the patient while performing fiberoptic intubation
Eligibility Criteria
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Inclusion Criteria
* aged 1 year to 3 years
* require general anaesthesia with tracheal intubation for surgical correction of the congenital or acquired pathology that created the difficult airway
Exclusion Criteria
* Allergy to drugs
1 Year
3 Years
ALL
No
Sponsors
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Alexandria University
OTHER
Responsible Party
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rehab zayed
Assisstant Professor of Anesthesia
Principal Investigators
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Rehab A. Abd Elaziz, Ass.Prof.
Role: PRINCIPAL_INVESTIGATOR
Alexandria University
Locations
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Rehab Abd Elraof Abd Elaziz
Alexandria, Smouha, Egypt
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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0304285
Identifier Type: -
Identifier Source: org_study_id
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