Recruitment

Recruitment Status
Not yet recruiting
Estimated Enrollment
Same as current

Summary

Conditions
  • Crackle
  • Lung Sound
  • Rhonchi
  • Wheezing
Type
Observational
Design
Observational Model: Case-OnlyTime Perspective: Prospective

Participation Requirements

Age
Younger than 318 years
Gender
Both males and females

Description

Multicenter, international - 2 EU sites (max. 1 in Poland) and a single US site. Trial centers and investigators will be identified and selected based on their clinical and research experience. The trial objective is to assess whether use of the StethoMe AI lung sounds analysis software provides cli...

Multicenter, international - 2 EU sites (max. 1 in Poland) and a single US site. Trial centers and investigators will be identified and selected based on their clinical and research experience. The trial objective is to assess whether use of the StethoMe AI lung sounds analysis software provides clinical benefit by improving the identification of abnormal lung sounds in the categories of wheezes, rhonchi, fine crackles and coarse as compared to pulmonary auscultation by experienced physicians (general practitioners (GPs) and pulmonologists). The recordings will be used to form a gold standard database of lung sounds as evaluated by an expert, independent panel according to the study protocol. The gold standard database will include approximately equal representation of wheezes, rhonchi, fine crackles and coarse crackles. Moreover, the database will also include recordings without any of the previous descripted pathological sounds. The results of these two analyses, by traditional physician listening and by the StethoMe AI software application, will be assessed for sensitivity and specificity to the gold standard database in detection of the four lung sounds and recordings without defined pathological sounds. The StethoMe AI will be considered to provide clinical benefit if it demonstrates statistically better sensitivity or specificity on any of the four lung sounds as compared to the traditional physician auscultation, together with F1 score analysis.

Tracking Information

NCT #
NCT04208360
Collaborators
Not Provided
Investigators
Not Provided