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N/A N=50

Correlation of Auscultatory Severity of Aortic Stenosis With Trans Thoracic Echocardiography

Aortic Stenosis

Enrolled (actual)
50
Serious AEs
0.0%
Results posted
Nov 2013
Primary outcome: Primary: Aortic Stenosis Acceleration Index Compared to Aortic Stenosis Severity — 21; 8; 1; 6 participants

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Tranthoracic Echocardiogram (Other); Cardiac Ascultation Recordings with Electronic stethoscope (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
United States Naval Medical Center, San Diego
Primary completion
Jun 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Aortic Stenosis Acceleration Index Compared to Aortic Stenosis Severity
21; 8; 1; 6

Summary

According to the 2006 ACC/AHA practice guidelines for valvular heart disease, patients with asymptomatic aortic stenosis(AS) should have screening transthoracic echocardiograms (TTE) performed annually for severe disease, every 1-2 years for moderate disease and every 3-5 years for mild disease. This results in a multitude of screening studies in the investigators patient population. 3M has developed a new stethoscope and phonocardiography software capable of identifying the peak intensity of the AS murmur and tracking it as it moves towards the second heart sound potentially indicating increasing severity of disease. Currently there exists no data to demonstrate that the aortic stenosis acceleration index (ASAI) correlates to disease severity or progression of disease. The ASAI measures the timing of the peak intensity of the systolic murmur and compares it to the total time in systole (S2-x/s2-s1) where s1 is the first heart sound; S2 is the second heart sound and x with the time between S1 and the peak intensity of the murmur. In this study the investigators propose to correlate the ASAI to standard TTE measurements of aortic stenosis severity.

Eligibility Criteria

Inclusion Criteria

  • Male and female subjects 18 years of age and older.
  • Subjects must have asymptomatic Aortic Stenosis documented by prior echocardiographic examination.
  • Subjects must be able to sit for auscultation examination.
  • Subject must be able to complete a TTE .
  • Subjects must voluntarily agree to participate in the study and sign the informed consent and healthcare information authorization forms.

Exclusion Criteria

  • Subjects with significant additional valvular heart disease.
  • Subjects with unrecordable heart sounds.
  • Subjects with known or who may have been previously diagnosed with congenital heart disease.
  • Subjects with atrial fibrillation.
  • Subjects with history of cardiac surgery.
  • Subjects who have conditions which the researcher feels may limit the recordability of the heart sounds or the accuracy of the echocardiogram.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01605669). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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