Recruiting

Shear Wave Velocity

Sponsor:

eMyosound SAS

Code:

NCT07215715

Conditions

HFpEF - Heart Failure With Preserved Ejection Fraction

HFmrEF

ATTR-CM (Transthyretin Amyloid Cardiomyopathy)

Left Ventricular Hypertrophy

Cardiac Amyloidosis

Eligibility Criteria

Sex: All

Age: 60+

Healthy Volunteers: Accepted

Study Details

Brief summary:

The goal of this observational study is to measure shear wave velocity (SWV) in patients with non-reduced left ventricular ejection fraction (LVEF) heart failure and left ventricular hypertrophy, with or without transthyretin amyloidosis with cardiomyopathy (ATTR-CM), and in control subjects without heart failure or cardiomyopathy.

The main question it aims to answer is:

• Can SWV be used to measure myocardial and liver stiffness in the study's target populations? Researchers will compare patients with ATTR-CM, patients without ATTR-CM, and a control group to determine the distributions of SWV in each population.

Participants will:

  • Have a standard cardiology assessment, including a physical exam, blood work, and an echocardiogram.
  • Undergo an investigational assessment with the eMyosound LYRA device to measure SWV in their myocardium and liver.
  • Have the investigational assessment repeated by a second observer to assess measurement reliability.

Conditions

HFpEF - Heart Failure With Preserved Ejection Fraction

HFmrEF

ATTR-CM (Transthyretin Amyloid Cardiomyopathy)

Left Ventricular Hypertrophy

Cardiac Amyloidosis

Study ID

NCT07215715

Start date

Sep 16, 2025

Status verified date

Oct, 2025

Completion date

Jul, 2026

Anticipated

Primary completion date

Jul, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 60+

Healthy Volunteers: Accepted

Inclusion Criteria:

Inclusion Criteria Common to all three Study Arms:

1. Male or female age ≥ 60 years
2. Signed informed consent and able to comply with protocol

Inclusion Criteria Common to the Heart Failure with non-reduced left ventricular ejection fraction (LVEF) with or without transthyretin amyloid cardiomyopathy (ATTR-CM) Arms:
3. Patients meeting the Universal Definition of Heart Failure \& HeartShare study criteria.
4. LVEF >40% on the last available imaging study
5. Left ventricular hypertrophy (LVH) defined as left ventricular mass index (mass/BSA) in female > 95 g/m², in male > 115 g/m² according to American Society of Echocardiography/European Association of Cariology (ASE/EAC) guidelines42 OR as interventricular septum (IVS) thickness ≥12 mm

Inclusion criterion specific to HF with non-reduced LVEF without ATTR-CM Arm:
6. Negative (grade 0) Pyrophosphate (PYP) scintigraphy within 24 months prior to the enrolment in the study OR Simple Score <643 OR negative endomyocardial biopsy

Inclusion criterion specific to HF with non-reduced LVEF with ATTR-CM Arm:
7. ATTR-CM objectively confirmed and classified at any time prior to the enrollment in the study, with monoclonal protein AL amyloidosis ruled out, according to American Heart Association (AHA) 2020 criteria

Inclusion criteria in Control Subjects:
8. No diagnosis of HF or cardiomyopathy according to the universal definition of Heart Failure
9. No diagnosis of Transthyretin amyloid cardiomyopathy (ATTR-CM) or Amyloid light-chain (AL) amyloidosis

Exclusion Criteria:

Exclusion criteria common to the three arms:

1. Pregnant OR pre-menopausal woman
2. Vulnerable patients
3. Acute Coronary Syndrome within 30 days
4. Heart rate greater than 130 beats/minute at the time of the measurements
5. Atrial fibrillation or flutter at the time of SWV measurement (history of AF is authorized provided they patient is in sinus rhythm at the time of the measurements)
6. Any clinically significant cardiac arrhythmia at the time of SWV measurement
7. Poor echogenicity preventing accurate ultrasound measurements
8. Patients with segmental wall motion abnormalities thought to be due to myocardial infarction.
9. Severe mitral or aortic valve disease (regurgitation or stenosis) excluded if the cause is other than ATTR (e.g., prolapse, endocarditis, prosthetic valve.)
10. Severe tricuspid valve disease (regurgitation or stenosis) excluded if the causes are other than ATTR.
11. Distance from skin to IVS ≥ 8 cm
12. Any prosthetic mechanical valve
13. Patients with mechanical cardiac assist devices other than pacemakers or defibrillators
14. Heart, lung, liver or kidney transplant history or expected in the next year
15. Severe renal impairment with eGFR < 15 mL/min/1.73m² or end-stage renal disease or patient on dialysis.
16. Presence of any competing life-threatening risk over the next 12 months
17. Complicated uncontrolled diabetes mellitus HbA1c ≥9% with target organ damage.
18. Uncontrolled and persistent high-blood pressure with diastolic pressure > 100 mmHg or systolic pressure > 160 mmHg at the time of the measurement.
19. Acute decompensated state such as volume overload, etc. in the opinion of the study investigator
20. Skin abnormalities, infections, or open wounds at the site of the SVW measurement
21. Liver disease, at least moderate

Exclusion criteria in both the HF with non-reduced LVEF with or without ATTR-CM Arms:
22. Known inherited cardiomyopathy, infiltrative cardiomyopathy (other than ATTR-CM for the study arm for ATTR-CM), cardiomyopathy from muscular dystrophies, cardiomyopathy with reversible causes (e.g., stress cardiomyopathy), hypertrophic cardiomyopathy or known pericardial constriction
23. History of treatment for ATTR-CM with Transthyretin (TTR) depleters

Exclusion criteria Specific to Control Subjects:
24. Any diagnosis of cardiomyopathy or HF, whatever the cause46
25. LVH based on LV mass index female >95 g/m², in male ≥115 g/m² OR IVS thickness ≥12 mm unless thought to be due to athlete's heart

Study Design

Enrollment

150 participants

Anticipated

Interventions and Outcome Measures

Arms

Heart Failure with LVEF > 40% and LVH with ATTR-CM

heart failure (HF) with left ventricular ejection fraction (LVEF) > 40% and left ventricular hypertrophy (LVH) with transthyretin amyloidosis with cardiomyopathy (ATTR-CM)

Heart Failure with LVEF > 40% and LVH, without ATTR-CM

Heart Failure with LVEF > 40% and LVH, without ATTR-CM

Control group of patients without heart failure or cardiomyopathy

Control group of patients without heart failure or cardiomyopathy.

Primary outcome measure

  • The primary outcome measures are the shear wave velocity (SWV) measurements extracted from the eMyosound LYRA device acquisitions. [ Time Frame: single study visit of a duration of approximatively 2.5 hours ]

Central Contacts and Locations

Central contacts

Director Clinical Operations

+33781549847clinical@emyosound.com

Locations

Massachusetts General Hospital

Recruiting

Boston, Massachusetts, United States, 02114

Contacts

Principal Investigator:

Hanna K Gaggin, M.D.

Brigham and Women's Hospital

Recruiting

Boston, Massachusetts, United States, 02116

Contacts

Principal Investigator:

Sarah Cuddy, M.D.

Boston Medical Center

Recruiting

Boston, Massachusetts, United States, 02118

Contacts

Principal Investigator:

Deepa M Gopal, M.D.

More Information

Sponsor

eMyosound SAS

Last update posted

Oct 20, 2025

Last verified

Oct, 2025

Keywords

  • Shear Wave Velocity
  • non-invasive ultrasound elastography
  • US Benchmarking Clinical Study
  • Heart Failure
  • Cardiac Amyloidosis
  • ATTR-CM

Trial information was received from ClinicalTrials.gov and was last updated on 2026-10-09. This information was provided to ClinicalTrials.gov by eMyosound SAS on 2025-10-20. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.