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OpenTrials
Completed

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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Key information

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

Point of Care Device; i-Stat Analyzer

Device

Primary outcomes

  1. Total Length of Stay

Secondary outcomes

  1. 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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