New blood test aims to slash unnecessary antibiotics in ER lung infections
NCT ID NCT05762302
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests a new blood test called MeMed BV in about 1,300 adults with suspected lower respiratory infections (like bronchitis or pneumonia) in the ER. The goal is to see if the test helps doctors prescribe antibiotics only when truly needed, reducing unnecessary use. Participants are randomly assigned to get the test result or standard care, and researchers track antibiotic prescriptions and health outcomes.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 1,316 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jan 2023
- Expected to finish
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Feb 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
INCLUSION CRITERIA * Patients eligible for inclusion are required to fulfill all of the following criteria: * Written informed consent must be obtained from the patient or his/her legal guardian. * 18 years of age or older. * Current disease duration ≤ 7 days. * Tactile fever or measured temperature ≥ 37.8°C (100°F) (any body site, any measurement device, including self-reported), either of them noted at least once within the last 7 days. * Clinical suspicion of bacterial or viral LRTI: At least one of the following respiratory signs or symptoms: cough (new or worsening), sputum production, dyspnea/shortness of breath, auscultatory abnormality (e.g. wheezing, rhonchi). * Clinician intent to prescribe antibiotics based on the currently available data. EXCLUSION CRITERIA Patients fulfilling any of the following criteria are not eligible for inclusion in the infectious cohort: * Systemic antibiotics within 72 hours prior to enrollment * Inflammatory disease (e.g., IBD, SLE, Rheumatoid arthritis, Kawasaki, other vasculitis) * Congenital immune deficiency (CID) * A proven or suspected infection on presentation with Mycobacterial (e.g., MAC, MABC), parasitic or fungal (e.g., Candida, Histoplasma, Aspergillus) pathogen * HIV, HBV, or HCV infection (self-declared or known from medical records) * Major surgery, trauma and\\or burns in the last 7 days * Pregnancy- self reported or medically confirmed * Active malignancy - Cancer diagnosed within the previous six months, recurrent, regionally advanced or metastatic cancer, cancer for which treatment had been administered within six months, or hematological cancer that is not in complete remission. * Patients with severe illnesses that affect life expectancy and quality of life such as end stage renal disease, end stage liver disease or severe COPD. * Clinician intent to hospitalize patient. * Patients with suspected concomitant infections (e.g. UTI, cellulitis, gastroenteritis, etc.) * Active treatment with immune-suppressive or immune-modulating therapies, including without limitations: Administration of PO\\IV\\IM high dose steroids \>1mg/kg/day prednisone (or equivalent) at some point in the past 10 days or daily continuous use of steroids \> 0.25 mg/kg/day in the past 7 days Monoclonal antibodies, anti-TNF agents Intravenous immunoglobulin (IVIG) Cyclosporine, Cyclophosphamide, Tacrolimus, Azathioprine, Methotrexate G/GM-CSF, Interferons •Considered unsuitable for the study by the study team
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
10 sites in 2 countries. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Carmel Medical Center
RECRUITINGHaifa, North, Israel
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Lin Medical Center
NOT_YET_RECRUITINGHaifa, Israel
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MCW
RECRUITINGMilwaukee, Wisconsin, 53226, United States
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Maimonides Medical Center
RECRUITINGBrooklyn, New York, 11219, United States
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Medical University South Carolina
RECRUITINGCharleston, South Carolina, 29425, United States
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Philadelphia Thomas Jefferson ED
RECRUITINGPhiladelphia, Pennsylvania, 19107, United States
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Stony Brook University Hospital
RECRUITINGStony Brook, New York, 11794, United States
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UT Southwestern Medical Center
RECRUITINGDallas, Texas, 75390, United States
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University of Florida-Jacksonville
RECRUITINGJacksonville, Florida, 32209, United States
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University of Kansas Medical Center
RECRUITINGKansas City, Kansas, 66160, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can simple checkups predict which kids will get severe pneumonia?