Automated Algorithm Based Analysis of Phonocardiograms of Newborns

Mitral Valve Prolapse Clinical Trial

Official title:

Automated Algorithm Based Analysis of Phonocardiograms of Newborns

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02105480
• Other study ID #: GRZ02 (AAAPN)
• Status: Completed
• Start date: November 2013
• Est. completion date: January 18, 2017

Study information

• Verified date: July 2018
• Source: CSD Labs GmbH
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

The purpose of this double-blind pivotal clinical utility study is to determine on a large patient population whether heart murmurs can be reliably detected with high sensitivity and specificity using a locked, automated algorithm-based phonocardiogram analysis (also referred to as computer aided auscultation (CAA)).

Each patient is auscultated and diagnosed independently by a medical specialist. Additionally, for each patient, an echocardiogram is performed as the gold-standard for determining heart pathologies. The CAA results are compared to the findings of the medical professionals as well as to the echocardiogram findings.

Hypothesis: The specific (locked) CAA algorithms used in this study are able to automatically diagnose pathological heart murmurs in premature babies and newborns with at least the same accuracy as experienced medical specialists.

Description:

The following registry procedures and quality factors have been implemented:

• Quality assurance plan, including

• data validation

• proper registration procedures

• regular site monitoring

• regular auditing

• Data checks to compare data entered into the registry against predefined rules for range or consistency with other data fields in the registry.

• Source data verification to assess the accuracy, completeness, or representativeness of registry data by comparing the data to external data sources (medical records and paper case report forms).

• Standard Operating Procedures to address registry operations and analysis activities, such as patient recruitment, data collection, data management, data analysis, reporting for adverse events, and change management.

• Sample size assessment to specify the number of participants or participant years necessary to demonstrate an effect.

• Statistical analysis plan describing the analytical principles and statistical techniques to be employed in order to address the primary and secondary objectives, as specified in the study protocol or plan.

• Plan for missing data to address situations where variables are reported as missing, unavailable, "non-reported," uninterpretable, or considered missing because of data inconsistency or out-of-range results.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 220
• Est. completion date: January 18, 2017
• Est. primary completion date: January 25, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A to 5 Days

Eligibility

Inclusion Criteria:

• any premature baby or newborn

• parental approval for study participation

Exclusion Criteria:

Related Conditions & MeSH terms

• Heart Murmurs
• Mitral Valve Prolapse
• Prolapse
• Systolic Murmurs

Intervention

Device:
• Computer aided auscultation (CAA)

Locations

Country	Name	City	State
Austria	University Hospital	Graz	Styria

Sponsors (1)

Lead Sponsor	Collaborator
CSD Labs GmbH

Country where clinical trial is conducted

Austria, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of correctly diagnosed heart murmurs through locked, independent algorithm based auscultation and traditional stethoscope based auscultation by medical experts	Each patient is screened and diagnosed regarding a potential heart murmur by a medical expert through standard stethoscope based auscultation. Heart sounds are recorded using an electronic stethoscope and analyzed and diagnosed independently (with no external input) by a locked algorithm. A final diagnoses for each patient is made by a medical expert by performing an echocardiogram, the gold standard method for heart murmur detection. The diagnoses of both the medical expert and the algorithm are finally compared to the echocardiogram based diagnosis (after completion of patient recruitment).	2 years (expected)