Study to Evaluate the Effectiveness of the Initial Specimen Diversion Device



Status:Recruiting
Conditions:Hospital
Therapuetic Areas:Other
Healthy:No
Age Range:19 - Any
Updated:4/2/2016
Start Date:July 2014

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A Matched, Open Label Study to Evaluate the Effectiveness of the MMT Initial Specimen Diversion Device in Reducing Blood Culture Contamination When Compared to Laboratory Standard Procedures

This is a matched, open label study to evaluate the Initial Specimen Diversion Device (ISDD)
in reducing the contamination rate in blood culture analysis. Blood culture data will be
derived from inpatient and/or outpatient settings in a variety of hospital departments (e.g.
ER, surgical, medical, etc.). Only samples that are collected via peripheral venipuncture
may be included in this study. The ISDD will be compared to current laboratory practices for
the collection of blood for culture purposes. Laboratory Standard Procedures (LSP) is
defined as collection of venipuncture blood for culture without an initial diversion method
to divert and sequester potential blood contaminants.


Inclusion Criteria:

- Adults >19 years old

Exclusion Criteria:

- Not a good candidate for direct-to-media (DTM) technique
We found this trial at
1
site
Emile St
Omaha, Nebraska 68198
(402) 559-4000
Univ of Nebraska Med Ctr A vital enterprise in the nation’s heartland, the University of...
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Omaha, NE
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