Artificial Intelligence Guided Echocardiographic Screening of Rare Diseases (EchoNet-Screening)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCedars-Sinai Medical Center

About this trial

Despite rapidly advancing developments in targeted therapeutics and genetic sequencing, persistent limits in the accuracy and throughput of clinical phenotyping has led to a widening gap between the potential and the actual benefits realized by precision medicine.

Recent advances in machine learning and image processing techniques have shown that machine learning models can identify features unrecognized by human experts and more precisely/accurately assess common measurements made in clinical practice.

The investigators have developed an algorithm, termed EchoNet-LVH, to identify cardiac hypertrophy and identify patients who would benefit from additional screening for cardiac amyloidosis and will prospectively evaluate its accuracy in identifying patients whom would benefit from additional screening for cardiac amyloidosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients who have a high suspicion for cardiac amyloidosis by AI algorithm

Disqualifiers

Patients who decline to be seen at specialty clinic

Patients who have passed away

Trial population

Patients who have a high suspicion for cardiac amyloidosis by AI algorithm

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • EchoNet-LVH screening for cardiac amyloidosis

    Other intervention

    An AI algorithm identifies LVH, low voltage, and high suspicion for cardiac amyloidosis. The intervention is the suspicion score. Patients with high suspicion score will be referred to specialty clinic for standard of care evaluation, screening, and treatment as determined by physicians.

Treatment groups

300 Participants
are divided into 1 treatment group
Group A: Artificial Intelligence Screening for Cardiac Amyloidosis1 intervention

Trial outcomes

Primary outcomes

1

Number of New Diagnoses of Cardiac Amyloidosis Found

From chart review, identification of patients who have a downstream diagnosis of cardiac amyloidosis

Time frame
6 months

Secondary outcomes

1

Number of New Diagnoses of TTR Amyloidosis Found

From chart review, identification of patients who have a downstream diagnosis of TTR amyloidosis

Time frame
6 months
2

Number of New Diagnoses of AL Amyloidosis Found

From chart review, identification of patients who have a downstream diagnosis of AL amyloidosis

Time frame
6 months

Other outcomes

Sponsors and contacts

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