Clinical trial
Ketamine/Propofol vs Ketamine Alone for Pediatric Fracture Reduction
NCT00490997 · London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's, Other · Completed
Key facts
| NCT number | NCT00490997 |
|---|---|
| Title | Ketamine/Propofol vs Ketamine Alone for Pediatric Fracture Reduction |
| Official title | A Prospective Randomized Double Blind Evaluation of Ketamine/Propofol vs Ketamine Alone for Pediatric Extremity Fracture Reduction |
| Lead sponsor | London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's, Other |
| Collaborators | University of Western Ontario, Canada |
| Status | Completed |
| Phase | Phase 4 |
| Study type | Interventional |
| Conditions | Fractures |
| Intervention type | Drug |
| Interventions | Ketamine only, Ketamine - Propofol |
| Enrollment | 140 |
| Start date | Jun 1, 2007 |
| Primary completion | Aug 1, 2008 |
| Completion | Aug 1, 2008 |
| First posted | Jun 25, 2007 |
| Last update posted | Aug 25, 2017 |
| Countries | Canada |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: