Bedside vs. Standard Microbiological Blood Culture Diagnostics - BEMIDIA Study
NCT ID: NCT03000049
Last Updated: 2016-12-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
500 participants
OBSERVATIONAL
2016-11-30
2017-09-30
Brief Summary
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Prospective observational, open-label mono-center study to compare a completely bedside blood culture diagnostics system (BACTEC blood culture system in combination with the Accelerate ID/AST System and Curetis Univero System) with standard blood culture diagnostics in patients with sepsis or septic shock.
Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Interventions
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bedside blood culture
Eligibility Criteria
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Inclusion Criteria
* informed written consent
Exclusion Criteria
* DNR-order
18 Years
ALL
No
Sponsors
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University Medicine Greifswald
OTHER
Responsible Party
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Sven-Olaf Kuhn
Sven-Olaf Kuhn MD
Locations
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Anesthesiology and Intensive Care Medicine Department, University of Greifswald, Germany
Greifswald, , Germany
Countries
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Central Contacts
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Facility Contacts
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Sven-Olaf Kuhn, MD
Role: primary
Matthias Gründling, MD
Role: backup
Other Identifiers
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SD_BK_1_ANI
Identifier Type: -
Identifier Source: org_study_id