Ketamine molecule:

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Ketamine Clinical Trials


A Prospective Randomized Double Blind Evaluation of Ketamine/Propofol vs Ketamine Alone for Pediatric Extremity Fracture Reduction


To see complete record on clinicaltrials.gov, please visit this link

Id: NCT00490997

Organisation Name: Lawson Health Research Institute

Overal Status: Completed

Start Date: June 2007

Last Update: August 25, 2017

Lead Sponsor: Lawson Health Research Institute

Brief 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.

Conditions:
  • Fractures


Total execution time in seconds: 0.46590304374695