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Study identifier: NCT06099795 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evaluation of Concordance Between Exhaled Air Test (eBAM-CoV) and RT-PCR to Detect SARS-CoV-2

Condition: SARS-CoV-2 Infection · COVID-19 · Coronavirus  ·  Sponsor: Centre Hospitalier Universitaire de Nīmes

PhaseNA
Planned participants250
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersYes

About this study

During the COVID-19 pandemic, testing primarily relied on the use of nasopharyngeal swabs to detect the SARS-CoV-2 virus, responsible for the disease. However, this technique has several limitations, including the variable quality of swabs, its invasive nature, and arbitrariness in the choice of the number of cycles. Furthermore, it does not allow for the detection of viral proteins. To overcome these limitations, researchers developed the eBAM-CoV test, patented for the detection of viral proteins in the exhaled air of COVID-19 patients. This portable device provides an immediate assessment of the "viral load" with both quantitative and qualitative results, showing promise for early virus detection. The researchers hypothesize that the eBAM-CoV test is likely to exhibit a satisfactory concordance with the reference RT-PCR test in the detection of COVID-19, especially among symptomatic patients or closed contacts.

This description comes directly from the study's public registry record.

Talk to the study team

Valérie COMPAN, PhD  ·  +33664915140  ·  vcompan@brains4d.com

Always discuss trial participation with your own doctor first.

Locations (2)

CHU de NIMESNîmes, FranceRecruiting
Université de NîmesNîmes, FranceNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06099795