drugset / Trial / NCT00490997

Ketamine/Propofol vs Ketamine Alone for Pediatric Fracture Reduction

NCT00490997 ↗

RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to compare Ketamine-Propofol with Ketamine-only in a double-blind, randomised, controlled trial in a paediatric emergency department. We believe that the combination of these two agents will provide a new and more effective option for procedural sedation in paediatric emergency department patients. The hypothesis of the study is that paediatric emergency department patients requiring procedural sedation for an isolated orthopaedic injury with Ketamine-Propofol will have reduced total sedation time, time to recovery, complications and improved satisfaction scores compared to patients receiving Ketamine alone.

Timeline

Start
2007-06
Primary completion
2008-08
Completion
2008-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Ketamine Small molecule 0.25 mg/kg Intravenous
Comparator Ketamine Small molecule 0.5 mg/kg Intravenous
Comparator Ketamine Small molecule 1 mg/kg Intravenous
Comparator Propofol Small molecule 0.5 mg/kg Intravenous
Comparator Propofol Small molecule 1 mg/kg Intravenous

Indications

No indication recorded.