Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02232750
Other study ID # 20141524
Secondary ID
Status Completed
Phase
First received
Last updated
Start date July 14, 2014
Est. completion date August 15, 2015

Study information

Verified date November 2021
Source Ohio State University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 1320
Est. completion date August 15, 2015
Est. primary completion date August 15, 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 90 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Wexner Medical Center at The Ohio State University Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
Ohio State University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary We are measuring CBC (complete blood count) and MNV (Mean Neutrophil Volume) Evaluate the clinical utility of CPD MNV as an aid in the diagnosis and risk assessment of Emergency Department patients for progression to sepsis, severe sepsis and septic shock. approximately 10 months