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COMPLETEDNCT03876535

Performance Evaluation of the Nanomix eLab® CRP, PCT, and LAC Assays With the Nanomix eLab System

The performance of the eLab C-Reactive Protein, Procalcitonin, and Lactate Assays will be demonstrated during a method comparison study in which venous whole blood and plasma samples are used. eLab re...

Lead sponsor: Nanomix•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Nanomix

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•Must be 18 years of age or older
•Must have provided written informed consent
•Admitted to ICU, Emergency Department or other medical wards for acute illness and observation of infection and meeting SIRS criteria (such as elevated heart rate, tachypnea, hypotension, fever, hypothermia, or elevated respiratory rate)

Exclusion Criteria

•Pregnant or nursing
•Admitted to ICU after trauma
•Admitted to ICU after surgery
•Cardiogenic shock

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: August 23, 2021Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment184

Start dateDec 2018

Last updatedAug 23, 2021

Condition

Locations shown

UCSF- San Francisco General Hospital

San Francisco, California

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: August 23, 2021Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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