Status:
RECRUITING
Correlation Between Sedation Depth Monitoring and Reflexes During Intravenous Anesthesia With Dexmedetomidine and Remifentanil in Children Undergoing Direct Laryngoscopy for Surgical Procedures
Lead Sponsor:
University Hospital, Antwerp
Conditions:
Laryngoscopy
Child
Eligibility:
All Genders
1-8 years
Brief Summary
This study evaluates the correlation between sedation depth monitoring obtained by NeuroSENSE ® NS 701 Monitor and reflexes during intravenous anesthesia in children undergoing direct laryngoscopy for...
Detailed Description
Direct laryngoscopy for invasive procedures in children is performed under general anesthesia with spontaneous or controlled ventilation.Preventing under-or over-sedation and titration of sedation acc...
Eligibility Criteria
Inclusion
- scheduled for elective direct laryngoscopy with surgical intervention, written informed consent of their parents or legal guardian.
Exclusion
- refusal of informed consent, known allergy for dexmedetomidine or remifentanil at start of anesthesia pulse oxygen saturation (SaO2) lower than 85%
Key Trial Info
Start Date :
October 23 2017
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 31 2025
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT03426579
Start Date
October 23 2017
End Date
December 31 2025
Last Update
January 22 2025
Active Locations (1)
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1
University hospital Antwerp
Edegem, Antwerp, Belgium, 2650