Biomarkers in Infection

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBeth Israel Deaconess Medical Center

About this trial

The purpose of this investigation is to evaluate how early biomarkers of infection and inflammation perform in identifying patients at risk for poor outcome in sepsis and septic shock.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Age 18 years of age or older

Confirmed or suspected infection

Age 18 years of age or older

A non-infectious clinical presentation to include

Disqualifiers

None

Trial population

Patients presenting to the Emergency Department with suspected infection as well as a non-infected control population.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

4,200 Participants
are grouped into 2 trial groups
Group A: Infected Group
Group B: Non-infected group

Trial outcomes

Primary outcomes

1

28 day in-hospital mortality

participants will be followed up for 28 days

Time frame
within 28 days after inclusion

Secondary outcomes

1

Organ Dysfunction assessed by Sepsis-related Organ Failure Assessment (SOFA) Score

Time frame
within 24 hours

Other outcomes

Sponsors and contacts

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