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MeMed BV® Test Evaluation in Adult Emergency Department Patients

Evaluation of the MeMed BV® Test in Adult Emergency Department Patients With Fever and Acute Respiratory Symptoms

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05706935
Enrollment
111
Registered
2023-01-31
Start date
2023-02-06
Completion date
2024-01-31
Last updated
2024-02-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory Infection, Respiratory Infection Bacterial, Respiratory Infections in Old Age, Respiratory Infection Virus

Brief summary

The goal of this observational study is to compare the results of a serum biomarker called the MeMed BV®, which is approved to help differentiate between bacterial and viral respiratory infections, to clinical diagnoses of adult emergency department patients presenting with recent fever and signs or symptoms of a respiratory infection. Active participation is completed during the emergency department visit and includes drawing blood, obtaining a sputum sample, and answering survey questions.

Detailed description

The MeMed BV® is a diagnostic test newly approved by the FDA to assess the likelihood of bacterial vs. viral respiratory infections based on protein biomarkers in blood. This study aims to identify the level of agreement between the results of the MeMed BV® (bacterial/viral) and the standard of care treatment received by the participant (e.g. antibiotics for patient diagnosed with bacterial pneumonia) in order to see if implementing the MeMed BV® into standard clinical care would potentially change diagnosis.

Interventions

DIAGNOSTIC_TESTMeMed BV® test

The MeMed BV® test is an automated semiquantitative immunoassay that measures three nonmicrobial (host) proteins (TRAIL, IP-10, and CRP) in serum samples and is intended for use in conjunction with clinical assessments and other laboratory findings as an aid to differentiate bacterial from viral infection.

Sponsors

University of Wisconsin, Madison
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults presenting to the emergency department * Subjective or objective fever within the past 7 days * Signs or symptoms of upper or lower respiratory tract infection within the past 7 days

Exclusion criteria

* Prisoner * Suspicion and/or confirmed diagnosis of infectious gastroenteritis/colitis * Active inflammatory disease * Congenital or acquired immune deficiency * Chronic fungal or parasitic infection * Infection with human immunodeficiency virus (HIV) * Hepatitis B virus (HBV) * Hepatitis C virus (HCV) * Infection with active tuberculosis (TB) * Significant trauma or burns in the last 7 days * Patients that have undergone major surgery in the last 7 days * Pregnancy * Active malignancy

Design outcomes

Primary

MeasureTime frameDescription
MeMed BV® test result and diagnostic concordanceEmergency department 1 day visitPercent agreement between result of MeMed BV® test (bacterial or viral respiratory infection) and antibiotic prescribing by emergency medicine doctor (which implies suspected bacterial infection)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026