Auscultate Obese Patients Using Electronic and Traditional Stethoscopes

NCT ID: NCT01665820

Last Updated: 2024-10-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-10-31

Study Completion Date

2012-12-31

Brief Summary

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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

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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.

Conditions

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Chest Pathology

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Auscultate with mechanical stethoscope

Cardiologist \& Medical Resident auscultate using mechanical stethoscope

Auscultate with electronic or mechanical stethoscope (3M Littmann)

Intervention Type DEVICE

Auscultate with electronic stethoscope

Cardiologist \& Medical Resident auscultate using electronic stethoscope

Auscultate with electronic or mechanical stethoscope (3M Littmann)

Intervention Type DEVICE

Interventions

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Auscultate with electronic or mechanical stethoscope (3M Littmann)

Intervention Type DEVICE

Other Intervention Names

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3M Littmann 3200 Electronic Stethoscope 3M Littman Cardiology III Mechanical Stethoscope

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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3M

INDUSTRY

Sponsor Role collaborator

Solventum US LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Egle Kalinauskiene, MD

Role: STUDY_DIRECTOR

Lithuanian University of Health Sciences

Locations

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Lithuanian University of Health Sciences

Kaunas, , Lithuania

Site Status

Countries

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Lithuania

Other Identifiers

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Study EM-05-012530

Identifier Type: -

Identifier Source: org_study_id

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