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Tests a wearable device for detecting wheeze in children and adults

Tests a wearable device that records lung sounds to detect wheeze in children and adults.

Plain-language title generated from the registry record
Registry title: AeviceMD for Detection of Wheeze in Pediatric and Adult Populations

Key facts

Where
The Bronx, United StatesSee the site

Where in United States

  • Montefiore Medical CenterThe Bronx, United StatesTaking people

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Trial details

Who runs it
Aevice Health Pte. Ltd.
Trial code
NCT06691971
Record updated
3 October 2025
Original description
Respiratory signs and symptoms consisting of wheeze, cough, and breathlessness are obtained in a manual fashion through history taking and physical examination by the healthcare professional. Auscultation of the lung assesses airflow through the trachea-bronchial tree and is helpful in diagnosing various respiratory disorders. AeviceMD is a wearable device that can acquire and process lung sounds, thus assisting in the detection of abnormal lung sounds. The primary objective of this study is to determine if AeviceMD can detect wheeze of pediatrics and adults as accurately as a physician through auscultation. The secondary objective is to investigate if AeviceMD can be used for remote auscultation of breath sounds.Read full original descriptionShow less

A Pilot Study to Assess Aevice Medical Device for Detection of Wheeze in Pediatric and Adult Populations

Respiratory signs and symptoms consisting of wheeze, cough, and breathlessness are obtained in a manual fashion through history taking and physical examination by the healthcare professional. Auscultation of the lung assesses airflow through the trachea-bronchial tree and is helpful in diagnosing various respiratory disorders. AeviceMD is a wearable device that can acquire and process lung sounds, thus assisting in the detection of abnormal lung sounds. The primary objective of this study is to determine if AeviceMD can detect wheeze of pediatrics and adults as accurately as a physician through auscultation. The secondary objective is to investigate if AeviceMD can be used for remote auscultation of breath sounds.

Inclusion: The subject is willing and/or parents/guardians are able to give informed consent for participation in the study; Male or Female, aged ≥ 3 years; Diagnosed with acute asthma exacerbation by an ED provider.

Exclusion: Any other significant disease or disorder which, in the opinion of the Investigator, may either put the subjects at risk because of participation in the study, or may influence the result of the study, or the subject's ability to participate in the study.

ClinicalTrials.gov NCT06691971