Evaluation of CPD MNV as an Aid in the Diagnosis and Risk Assessment of Sepsis (Protocol # Sepsis 1-14)
NCT ID: NCT02232750
Last Updated: 2021-11-03
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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COMPLETED
1320 participants
OBSERVATIONAL
2014-07-14
2015-08-15
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Patients presenting to the Emergency Department
* CBC (Complete Blood Count) with differential testing performed and CPD data retrieved
Exclusion Criteria
18 Years
90 Years
ALL
Yes
Sponsors
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Ohio State University
OTHER
Responsible Party
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Elliott Crouser MD
Medical Director, Intensive Care Unit
Locations
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Wexner Medical Center at The Ohio State University
Columbus, Ohio, United States
Countries
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References
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Crouser ED, Parrillo JE, Seymour C, Angus DC, Bicking K, Tejidor L, Magari R, Careaga D, Williams J, Closser DR, Samoszuk M, Herren L, Robart E, Chaves F. Improved Early Detection of Sepsis in the ED With a Novel Monocyte Distribution Width Biomarker. Chest. 2017 Sep;152(3):518-526. doi: 10.1016/j.chest.2017.05.039. Epub 2017 Jun 15.
Other Identifiers
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20141524
Identifier Type: -
Identifier Source: org_study_id