Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Analgesia
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: The study population will receive a target dose of intranasal CT001 corresponding to sufentanil 0.5 mcg/kg + ketamine 0.5 mg/kg (and an additional dose 10 -15 minutes after, if needed) prior to an elective surgical, procedure.Masking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 1 years and 17 years
Gender
Both males and females

Description

Not Provided

Not Provided

Tracking Information

NCT #
NCT04897750
Collaborators
Not Provided
Investigators
Principal Investigator: Torsten Lauritsen, MD Department of Anaesthesiology, The Juliane Marie Centre Copenhagen University Hospital