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UnknownNCT04426552

Dexmedetomidine Versus Sevoflurane in Children With Anticipated Difficult Intubation

Dexmedetomidine Versus Sevoflurane Inhalation for Fibreoptic Nasotracheal Intubation in Children With Anticipated Difficult Intubation

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Alexandria University · Academic / Other
Sex
All
Age
1 Year – 3 Years
Healthy volunteers
Not accepted

Summary

difficult problem in the paediatric age group because of their small mouth opening and un-cooperativeness.Currently used methods of sedation for fibreoptic intubation such as benzodiazepines, propofol or opioids may cause respiratory depression, especially when used in high doses

Detailed description

Dexmedetomidine, an a2-agonist, has none-to-minimal respiratory depressant effects, which is clearly a great advantage in handling a critical (unstable, difficult) airway while inducing sedation in both adult and infants. The aim is to compare intubation conditions between dexmedetomidine and sevoflurane inhalation during fibreoptic intubation in pediatric patients with an anticipated difficult intubation

Conditions

Interventions

TypeNameDescription
DRUGdexmedetomidinewill 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
DRUGsevofluranepreoxygenated 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

Timeline

Start date
2020-06-01
Primary completion
2020-09-20
Completion
2020-10-20
First posted
2020-06-11
Last updated
2020-06-12

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT04426552. Inclusion in this directory is not an endorsement.