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

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

1320 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-07-14

Study Completion Date

2015-08-15

Brief Summary

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The investigators hypothesize that CPD parameters will provide improved prediction of sepsis compared to currently employed laboratory parameters. These studies hold the potential to shape practitioner guidelines and improve the timeliness and accuracy with which patients with sepsis are treated today.

Detailed Description

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Conditions

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Sepsis, Severe Sepsis and Septic Shock

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Adult (≥18 to 90 years)
* Patients presenting to the Emergency Department
* CBC (Complete Blood Count) with differential testing performed and CPD data retrieved

Exclusion Criteria

* Previously enrolled in this study
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Ohio State University

OTHER

Sponsor Role lead

Responsible Party

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Elliott Crouser MD

Medical Director, Intensive Care Unit

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Wexner Medical Center at The Ohio State University

Columbus, Ohio, United States

Site Status

Countries

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United States

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.

Reference Type DERIVED
PMID: 28625579 (View on PubMed)

Other Identifiers

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20141524

Identifier Type: -

Identifier Source: org_study_id