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Unmasking the Prevalence of AC in an Unselected Echocardiographic Population (AC-TIVE)

U

University of Trieste

Status

Unknown

Conditions

Amyloid Cardiomyopathy

Treatments

Diagnostic Test: Amyloid Cardiomyopathy

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04738266
199_2019

Details and patient eligibility

About

This study will investigate the prevalence of echocardiographic red-flags of amyloid cardiomyopathy (AC) in patients undergoing clinically-indicated echocardiography (observational phase) and the prevalence of AC among AC-suggestive echocardiograms (interventional phase).

Full description

Prospective multicenter Italian survey consisting of two phases: observational (echocardiographic screening for amyloid cardiomyopathy among patients ≥ 55 years undergoing clinically-indicated echocardiography) and interventional (specific clinical and instrumental work-up to detect the prevalence of amyloid cardiomyopathy among amyloid cardiomyopathy-suggestive echocardiograms).

Enrollment

381 patients

Sex

All

Ages

55 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

All the following:

  • Interventricular septum thickness ≥ 13 mm in men and ≥ 12 mm in women;
  • Left ventricular ejection fraction ≥ 50%;
  • Indexed end-diastolic left ventricular volume ≤ 85 mL/m2.

AND

At least one of the following criteria:

  • "Granular sparkling" appearance of the myocardium defined granular texture with uniform increased brightness of echo-reflections;
  • Pericardial effusion regardless of severity;
  • Increased interatrial septum thickness (> 5 mm);
  • Restrictive filling pattern (Dec. Time E wave <120 ms or Dec. Time E wave ≤150 ms e E/A ratio ≥2) or increased ventricular filling pressures (E/E'15);
  • Speckle tracking derived global longitudinal strain with apical sparing pattern;
  • Increased thickness (> 5 mm) of mitral and tricuspid valve leaflets.

Exclusion criteria

  • Patients aged < 55 years or > 100 years
  • Echocardiography performed due to known or suspected amyloid cardiomyopathy;
  • Echocardiography performed due to known hypertrophic cardiomyopathy or phenocopies;
  • Refuse to sign the informed consent to the study

Trial contacts and locations

16

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Data sourced from clinicaltrials.gov

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