Study to Evaluate the Effectiveness of the Initial Specimen Diversion Device

Completed · Not applicable

Conditions studied: Septicemia

In brief

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.

Key facts

Study ID

NCT02102087

Run by

Magnolia Medical Technologies, Inc.

People needed

971

Starts

2014-07-01

Expected to finish

2015-10-01

Last updated by the study team

2017-08-11

Who can join

Age: 19 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults >19 years old

You may not qualify if…

• Not a good candidate for direct-to-media (DTM) technique

Where it is running

• University of Nebraska Medical Center — Omaha, Nebraska, United States

Full record on ClinicalTrials.gov

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