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DI-SOUND Study: Digital Heart Sound Classification in Pediatric Patients

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Summary

NIH registered an observational clinical trial (NCT07542509) titled 'DI-SOUND Study' to develop a digital classifier using commercially available digital stethoscopes to categorize pediatric heart sounds as physiological or pathological. The proof-of-concept study aims to address limitations in current neonatal screening for congenital cardiovascular diseases, including sensitivity failures and false positives. The trial is registered as observational with no prospective assignment.

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What changed

A new observational clinical trial has been registered on ClinicalTrials.gov under NCT07542509. The DI-SOUND Study is a proof-of-concept project to develop a machine learning classifier that uses commercially available digital stethoscopes to categorize pediatric heart sounds. The research addresses current limitations in neonatal screening procedures for duct-dependent congenital cardiovascular diseases.\n\nAffected parties include clinical investigators, pediatric cardiologists, and healthcare institutions involved in neonatal cardiac screening. The trial registration represents an informational entry with no compliance obligations or regulatory deadlines for external parties.

Archived snapshot

Apr 22, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Digital diagnoSis of Cardiac sOUNd in peDiatric Patients [DI-SOUND Study]

Observational NCT07542509 Kind: OBSERVATIONAL Apr 21, 2026

Abstract

Neonatal screening procedures for potentially life-threatening congenital cardiovascular diseases (i.e., duct-dependent systemic or pulmonary circulation), currently implemented at the national level, rely primarily on cardiovascular physical examination performed by a neonatologist. More recently, this approach has been complemented by the assessment of hemoglobin oxygen saturation at both the upper and lower extremities (pre- and post-ductal saturation) in order to improve diagnostic sensitivity, although this practice has not yet been uniformly adopted nationwide. Converging evidence indicates that these screening strategies are affected by significant limitations in both sensitivity (failure to identify affected individuals) and specificity (false-positive findings in healthy subjects). These limitations are associated with substantial overall costs for the healthcare system. Failure to correctly identify affected neonates may result in increased morbidity and mortality, whereas overdiagnosis leads to unnecessary second-level diagnostic investigations and imposes a considerable psychological burden on families, who remain understandably anxious until diagnostic confirmation is achieved.

The aim of the present research project (proof-of-concept study) is to develop a digital classifier capable to categorize heart sounds with commercially available digital stethoscopes into a binary classification system distinguishing physiological from pathological sounds. The derivat...

Conditions: Cardiac Disease, Auscultation of Heart, Machine Learning

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Last updated

Classification

Agency
NIH
Published
April 21st, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07542509

Who this affects

Applies to
Clinical investigators Healthcare providers
Industry sector
6211 Healthcare Providers
Activity scope
Clinical research Medical device development
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Medical Devices Artificial Intelligence

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