NCT Number: NCT00285285
Point of Care Device Use in the Pediatric Emergency Department
To compare the effect of "point-of-care" (POC) analysis of blood work with traditional laboratory methods on length of stay in a pediatric emergency department (PED).
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Conditions
Age range
1 day–21 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
About this study
This study was a prospective, randomized controlled study of patients requiring blood work that a POC device was capable of performing. Length of time spent at various timepoints were prospectively recorded by a dedicated research assistant after randomization.
Who can participate
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Clinically requiring bloodwork capable by the POC device
Exclusion criteria
- Requiring other bloodwork such as medication levels, WBC
Treatment and study plan
Primary outcomes
-
Total Length of Stay
Secondary outcomes
-
Time length for results return, disposition decision, time in ED proper
Sponsors and collaborators
Lead sponsor
Yale University
Other
Collaborators
- Karen A. Santucci
- M. Douglas Baker
- i-Stat Corporation
Registry information
Official study title
A Randomized Trial to Assess the Efficacy of Point-of-Care Testing in Decreasing Length of Stay in a Pediatric Emergency Department
Important dates
- Study start
- 2004
- Study completion
- 2004
- First posted
- Feb 1, 2006
- Registry last updated
- Feb 1, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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