An observational study in Sepsis, Severe Sepsis and Septic Shock, sponsored by Ohio State University. Completed at 1 site in United States. Open to participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2021-11-03.
Sponsored by Ohio State University · Observational
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.
1,899 studies on the registry are indexed under Sepsis; 462 are open to participants now.
This study's enrollment of 1,320 is above the median of 160 across 931 observational studies indexed under Sepsis.
Browse Sepsis studies →Ohio State University is the lead sponsor of 640 studies on the registry; 144 are open to participants now.
Of its 60 completed or terminated interventional studies of FDA-regulated products, 45 (75%) have results posted.
Counted across the registry records on this site, refreshed daily.
Emergency Department
Exclusion Criteria:
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.
Time frame: approximately 10 months
This study is completed, as verified in Nov 2021. You cannot join it, but the record below documents what was studied.
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Ohio State University