CClinicalTrials.gg
Status unknownNCT04456582ELAST-2DUpdated Jul 2, 2020

Noninvasive Assessment of Myocardial Stiffness by 2D-SWE Ultrasound Technique (Bidimensional Shear Wave Elastography) in Patients With Transthyretin Amyloidosis

An interventional study of Shear wave elastography in Amyloidosis, sponsored by Fábio Fernandes. Status unknown at 1 site in Brazil. Open to participants aged 18 Years to 85 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2020-07-02.

Sponsored by Fábio Fernandes · Not applicable, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Jun 2020), so the status shown — last known as Recruiting — may be out of date.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Non-randomized
Ages
18 Years to 85 Years
Sex
All
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Study summary

Amyloidosis by mutation of the transthyretin gene (ATTRh) is part of a group of diseases in which the deposit of structurally abnormal proteins (amyloid fibrils) affects multiple organs such as: liver, kidney, eyes, nervous system, gastrointestinal tract and heart, and, finally, it increases the morbidity and mortality of affected patients. This deposit in the myocardium is manifested syndromically as heart failure with preserved or slightly reduced systolic function, and important diastolic dysfunction. The analysis of diastolic function comprises two components: the assessment of active relaxation, dependent on preload and afterload, and the assessment of the passive properties of the tissue - its hardness or rigidity. Myocardial stiffness represents an important parameter for diagnosis and prognosis, but its evaluation is not included in conventional echocardiography. Cardiac elastography has recently been proposed as a non-invasive diagnostic modality to assess myocardial stiffness.

02

Conditions studied

  • Amyloidosis

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Keywords

  • Amyloidosis
  • Elastography
  • Cardiac
  • Miocardical stiffness
03

In context

Amyloidosis

491 studies on the registry are indexed under Amyloidosis; 135 are open to participants now.

This study's planned enrollment of 60 is above the median of 40 across 304 interventional studies indexed under Amyloidosis.

Browse Amyloidosis studies →

Lead sponsor

Fábio Fernandes is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Documented diagnosis of HRTR with and without cardiac involvement.
  • For the definition of cardiac involvement by ATTRh, all the criteria below must be presented:

    • Pathogenic mutation of TTR consistent with ATTRh.
    • Evidence of cardiac commitment by echocardiography or nuclear magnetic resonance with measurement of the interventricular septum at the end of diastole (SIVd)> 12mm or / and medical history of heart failure, and / or levels of troponin and / or BNP above the reference value without another more likely cause.
    • Amyloid deposit in cardiac or extra-cardiac tissue (eg, abdominal fat aspirate, salivary gland, connective sheath of the median nerve) confirmed by congo red staining or presence of grade 2 or 3 myocardial scintigraphy (DPD-CT) of cardiac uptake, in cases where the presence of monoclonal gammopathy of undetermined significance (MGUS) was ruled out.
    • In the presence of MGUS, confirmation of the TTR protein in the tissue is necessary through immunohistochemistry (IHC) or mass spectrometry.

Exclusion criteria

Exclusion Criteria:

  • Presence of another type of cardiomyopathy such as hypertension, valve or ischemic heart disease (eg, previous myocardial infarction documented with myocardial necrosis markers and electrocardiographic changes).
  • Presence of diseases other than cardiac amyloidosis, impairing the assessment of functional capacity, such as chronic obstructive pulmonary disease, severe arthritis or peripheral arterial disease, recent or planned orthopedic procedure during the course of the study (eg, spine surgery or under lower limbs) that impairs walking in the 6-minute test evaluation.
  • Acute coronary heart disease or unstable angina in the past 3 months
  • Report of disease of the sinus or atrioventricular node with indication of a pacemaker, but with no intention of implantation.
  • Presence of untreated hypothyroidism or hyperthyroidism.
  • Previous heart, liver or other organ transplant.
  • Presence of neoplasia in the last 3 years, except for basal and squamous cell carcinomas of skin or cervical cancer in situ previously treated.
  • Presence of other medical conditions or comorbidities that, in the investigator's opinion, could interfere with the course of the study or the interpretation of the data.
  • Pregnancy.
  • History of alcohol abuse in the last 2 years or excessive daily alcohol intake (for women, more than 14 units per week; for men, more than 21 units of alcohol per week [unit: one glass of wine (125ml) = one dose of distillate = 332.5ml of beer).
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    Amyloidosis transthyretin with cardiac commitment

    Shear wave elastography (SWE) will be used to evaluate to assess miocardial elasticity.

    Procedure: Shear wave elastography

  • Experimental
    Amyloidosis transthyretin without cardiac commitment

    Shear wave elastography (SWE) will be used to evaluate to assess miocardial elasticity.

    Procedure: Shear wave elastography

  • Placebo comparator
    Healthy subjects

    Shear wave elastography (SWE) will be used to evaluate to assess miocardial elasticity.

    Procedure: Shear wave elastography

Interventions

  • ProcedureShear wave elastography

    The elastographic technique by ultrasound (USE), shear waves or shear wave elastography (SWE), quantitatively evaluates tissue stiffness by mapping the propagation of acoustic waves (shear waves), in a non-invasive manner and without emission of ionizing radiation. Their speeds are tracked by the ultrasound equipment after tissue deformation occurs, generated by pulses of acoustic radiation (ARFI) of the transducer itself. Assuming the correlation between tissue stiffness and increased acoustic propagation speeds, it is possible to describe mathematically the elasticity of tissues by measuring specific acoustic waves.

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What researchers measure

Primary outcomes

  1. Dyastolic miocardical elasticity

    Diastolic myocardial elasticity could provide a more direct response to the constitution of the tissue and allow a simple, safe and diastolic function assessment and early initiation of specific treatment.

    Time frame: Around 6 months

07

Study locations

1 of 1 sites recruiting
  • University of Sao Paulo Medical School - The Heart Institute
    Sao Paulo, 05403-000, Brazil
    • Fabio Fernandes, MD, PhD · Contact · fabio.fernandes@incor.usp.br · +551126615057
    • Aristoteles C. Neto, Bachelor · Contact · aristotelesalencar@gmail.com · +5511960993262
    • Fabio Fernandes, MD, PhD · Principal investigator
    • Aristoteles C. Neto, B.S. · Sub investigator
    • Caio Cafezeiro, B.S. · Sub investigator
    • Joao H. Rissato, B.S. · Sub investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2020, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT04456582
Lead sponsor
Fábio Fernandes
Collaborators
Pfizer
Responsible party
Fábio Fernandes (Full Professor, University of Sao Paulo General Hospital) — Sponsor-investigator
First posted
Jul 2, 2020
Start date
Jun 3, 2020
Primary completion
Jan 31, 2021 (estimated)
Completion
May 29, 2021 (estimated)
Last update
Jul 2, 2020

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jun 2020. You cannot join it, but the record below documents what was studied.

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