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Recruiting NCT07270744

Data Collection Using Eko Devices in a Clinical Setting

— Observational Lung Diseases

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Eko digital stethoscopes.
Who it may be relevant to
Registry conditions: Lung Diseases. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
India
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Data Collection Using Eko Digital Devices in a Clinical Setting

Overview

The main objectives of the study are to: train and validate binary classifiers for wheeze, coarse crackle, fine crackle, rhonchus, stridor, rales, and cough, as well as determine correspondence between type/location of adventitious lung sound and type of pulmonary condition.

Interventions

  • Device Eko digital stethoscopes
    Use of the Eko CORE 500 digital stethoscope and 3M Littmann CORE Digital Stethoscope to listen for and record lung sounds.

Primary outcome measures

  • Primary Objective: Collection of Lung Sound Recordings to Explore Machine Learning Algorithm for Classifying Adventitious Lung Sounds [Time frame: 14-15 months]

Eligibility criteria

Inclusion criteria

  • Patients suspected or diagnosed lower respiratory condition OR Presence of wheeze, coarse crackle, fine crackle, rhonchus, stridor, rales, and cough discovered during routine auscultation
  • Normal patients with no adventitious lung sounds
  • Adults patients, over 18 years old
  • Able to provide verbal consent

Exclusion criteria

  • Patients unable to have multiple recordings taken on chest and back (e.g. compromised mobility)
  • Patients on mechanical ventilation
  • Patients unwilling or unable to provide informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

India · 1 center
  • P. D. Hinduja Hospital and Medical Research Centre — Mumbai

Identifiers

NCT: NCT07270744 · 2025.6

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗