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Auscultate Obese Patients Using Electronic and Traditional Stethoscopes

Study EM-05-012530 Benefit of Auscultation With 3M™ Littmann® 3200 Electronic Stethoscope to Diagnose Murmurs and Heart Pathologies in Overweight and Obese Patients With Increased Layers of Adipose Tissue

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01665820
Enrollment
30
Registered
2012-08-15
Start date
2012-10-31
Completion date
2012-12-31
Last updated
2024-10-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chest Pathology

Keywords

chest, pathology

Brief summary

Auscultating Obese patients using the 3M Littmann Electronic Model 3200 Stethoscope is more effective in identifying referrable murmurs than using a traditional stethoscope.

Detailed description

Study will enroll subjects who have greater than 30 BMI ratings. Each subject will receive 4 auscultation examinations. Two auscultations will be done by a cardiologist using both an acoustic traditional stethoscope and an electronic stethoscope. Two additional auscultations will be done by a 3rd year medical resident also using both an acoustic traditional stethoscope and an electronic stethoscope. All determinations will be compared to echocardiography results.

Interventions

DEVICEAuscultate with electronic or mechanical stethoscope (3M Littmann)

Sponsors

3M
CollaboratorINDUSTRY
Solventum US LLC
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Greater or equal than 18 years of age * Referred for an echocardiogram * obese, as defined as having a BMI greater than 30 * volunteers to participate in study * agrees to provide copy of echocardiogram exam report

Exclusion criteria

-Investigator believes subject should not be included or is unsuitable for inclusion

Design outcomes

Primary

MeasureTime frame
Most severe cardiac lesion identified by auscultation & echocardiography0-4 days

Secondary

MeasureTime frame
Secondary cardiac lesion identified by auscultation & echocardiography0 - 4 days
Other heart sounds identified by auscultation & echocardiography0 - 4 days

Countries

Lithuania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026