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A Prospective Study to Assess the Utility of CA-4F in a Canadian Cardiology Setting

A Prospective Study to Assess the Utility of CA-4F in a Canadian Cardiology Setting

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05210010
Enrollment
8
Registered
2022-01-27
Start date
2021-11-01
Completion date
2022-05-31
Last updated
2022-01-27

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

Conditions

Transthyretin Amyloid Cardiomyopathy (ATTR-CM)

Brief summary

This study will assess whether CA-4F can improve diagnosis of ATTR-CM in a community cardiology setting when used to screen electronic medical record data for patients suitable for follow-up investigations.

Detailed description

This is a prospective multicentre observational study to assess whether CA-4F can improve diagnosis of ATTR-CM in a community cardiology setting when used to screen electronic medical record data for patients suitable for follow-up investigations. The algorithm will be used to screen electronic health records of participating cardiologists for patients suitable for PYP scans to investigate potential ATTR-CM and determine its positive predictive value. Input parameters to the algorithm will be extracted from the pseudonymized electronic health records of patients who visited participating cardiologists in the 12 months preceding their enrolment. The records of patients with elevated pre-test likelihood of ATTR-CM will be queried for Canadian Heart Failure Society red flag symptoms to facilitate clinical review. Participating cardiologists will review the red flag symptoms and electronic health records of patients with elevated pre-test likelihoods and document whether further investigation with PYP is clinically justified with supporting rationale. Patients for which further investigation is clinically justified will be referred for confirmatory testing and the results of additional investigations will be documented. The positive predictive values of moderate, high and very high CA-4F Risk Scores will be calculated by determining the percentage of those patients for which further investigations were performed and resulted in diagnosis of ATTR-CM.

Interventions

DEVICECA-4F

The study intervention is the CA-4F algorithm developed by Ensho Health. The algorithm is a process for converting input parameters to a CA-4F Risk Score intended to facilitate clinical prioritization of patients suitable for follow-up investigation for ATTR-CM. The algorithm is applied using the CA-4F Likelihood Estimator which encodes it in software and records its outputs. The CA-4F Likelihood Estimator is controlled through a graphical user interface called the CA-4F Controller. The CA-4F Likelihood Estimator and its Controller are Class I medical devices in Canada registered under the Medical Device Establishment License of Ensho Health (license 16208).

Sponsors

Ensho Health Intelligent Systems Inc.
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

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

Inclusion criteria

* Licensed cardiologist in the Canadian provinces of Ontario, Saskatchewan or British Columbia * Outpatient cardiology practice with ≥1,200 unique patients annually * Have used an electronic medical record system for ≥36 months from enrollment * Currently subscribed to the Advanced Computing Platform by Ensho Health or using a cloud-hosted electronic medical record system compatible with the Apollo Electronic Data Capture System * Experience with the clinical management of ATTR-CM * Access to PYP scanning for follow-up investigations * Previous participation in clinical studies

Exclusion criteria

* Predominantly hospital-based cardiology practice * Have used an electronic medical record system for \<36 months from enrollment * Electronic medical record system incompatible with the Apollo Electronic Data Capture system * No prior experience with the clinical management of ATTR-CM * No access to PYP scanning for follow-on investigations * No prior participation in clinical studies

Design outcomes

Primary

MeasureTime frameDescription
Clinical utility of CA-4FSix monthsPositive predictive value of moderate or greater CA-4F Risk Score as confirmed by PYP scan

Secondary

MeasureTime frameDescription
Optimal threshold for clinical useSix monthsPositive predictive values of moderate, high, very high, and high or greater CA-4F Risk Scores as confirmed by PYP scan

Other

MeasureTime frameDescription
Impacts of CA-4F on age at first diagnosisSix monthsDifference in age at diagnosis of patients diagnosed through the study and patients of participating cardiologists previously diagnosed with ATTR-CM
Impacts of CA-4F on rate of diagnosis in priority subgroupsSix monthsDifference in biological sex distribution and left ventricular wall thickness measurements of patients diagnosed through the study and patients of participating cardiologists previously diagnosed with ATTR-CM

Countries

Canada

Outcome results

None listed

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