Multimodality Cardiac Imaging for Disease Progression in ATTR-CM

NCT ID: NCT07112066

Last Updated: 2025-12-09

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-10-20
• Study Completion Date: 2027-06-30

Brief Summary

The goal of this clinical trial is to investigate whether new imaging techniques can help us to better understand the cardiac amyloidosis. The disease can be slowed down with various medications (e.g., tafamidis, acoramidis, or vutrisiran). However, treatment is not effective in all patients-in about one-third of cases, the disease continues to progress. So far, we know little about the exact causes of this and what biological changes occur in the heart muscle.

The main question it aims to answer is:

Will new imaging techniques help us understand the course of the cardiac amyloidosis?

Participants will have additional examinations:

• At the beginning of the study: one additional heart ultrasound examination, one cardiac MRI and one cardiac PET, blood examination during the regular examination, questionnaires.
• After a year: one additional heart ultrasound examination, one cardiac MRI and one cardiac PET, blood examination during the regular examination.

Time required:

• Heart ultrasound examination: 5-10 Minutes
• Cardiac MRI: 2 hours
• Cardiac PET: 2 hours
• Questionnaires: 5-10 Minutes.

Detailed Description

Experimental Design The study design is an open label prospective longitudinal study with serial imaging at baseline and after 12-month follow-up. The entire study population will include 50 participants with cardiac ATTR amyloidosis, as recently defined by multi-societal criteria.

Conventional markers of disease progression

These markers are collected during routine clinical follow-up of patients in our Outpatient Clinic. The markers are divided into three domains and include the following outcomes:

• Clinical and functional: any heart failure hospitalization, NYHA class, Kansas City Cardiomyopathy Questionnaire, 6-minute walk test;
• Laboratory biomarkers: NT-proBNP, troponin, creatinine;
• Imaging and ECG: LV wall thickness, diastolic dysfunction, LVEF, stroke volume, global longitudinal strain, conduction disturbance.

Data Analysis Plan Power calculation for sample size is challenging as no previous study has evaluated the response of our endpoints in myocardial FAPI uptake or serum BMP4 concentration to tafamidis. We therefore focused sample size calculation of echocardiographic myocardial stiffness. Based on our own preliminary data, we estimate median baseline values for myocardial stiffness of 2.6 m/s [IQR, 1.7-3.8] in cardiac amyloidosis. Disease progression is expected in about 30% of participants. While myocardial stiffness is expected to remain unchanged in cardiac amyloidosis without disease progression a 20% relative increase (i.e. 0.5 ± 0.5 m/s) is considered in cardiac amyloidosis with disease progression. A sample size of 40 participants (i.e. 30 participants without and 10 participants with disease progression) has a statistical power of 80% to predict a difference in response of myocardial stiffness to tafamidis.

Non-normally distributed, paired data of repeated measures (i.e. longitudinal changes per group) are compared by Wilcoxon signed rank test. Non-normally distributed unpaired data of changes (i.e. longitudinal changes between groups) are compared by Mann-Whitney test. The correlations are compared by a z-test on Fisher z-transformed correlation coefficients.

Conditions

Amyloidosis Cardiac

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

18F-FAPI PET/CT

Additional imaging including 18F-FAPI PET/CT is performed

Group Type: EXPERIMENTAL

FAPI tracer

Intervention Type: DIAGNOSTIC_TEST

18F-FAPI-74 PET/CT, cardiac MRI, echocardiography and blood sample for BMP5 serum concetration is performed at baseline and 12-month follow-up.

Interventions

FAPI tracer

18F-FAPI-74 PET/CT, cardiac MRI, echocardiography and blood sample for BMP5 serum concetration is performed at baseline and 12-month follow-up.

Intervention Type: DIAGNOSTIC_TEST

Eligibility Criteria

Inclusion Criteria

• Participants with cardiac ATTR amyloidosis, as recently defined by multi-societal criteria, who are about to start tafamidis at the University Hospital Zurich

Exclusion Criteria

• Any other disease-modifying therapy (e.g. patisiran)
• Ongoing supraventricular arrhythmia
• Ventricular pacing
• Prior septal myocardial infarction

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Olga Mayenfisch Stiftung, Zurich, Switzerland

UNKNOWN

Sponsor Role: collaborator

University of Zurich

OTHER

Sponsor Role: collaborator

Dominik Benz

OTHER

Sponsor Role: lead

Responsible Party

Dominik Benz

PD Dr. med. Dominik C. Benz

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Dominik C Benz, MD

Role: PRINCIPAL_INVESTIGATOR

Universität Zürich

Locations

University Hospital Zurich

Zurich, Canton of Zurich, Switzerland

Site Status: RECRUITING

Countries

Switzerland

Central Contacts

Dominik C Benz, PD Dr. med.

Role: CONTACT

dominik.benz@usz.ch

+41432531191

Facility Contacts

Dominik Benz, PD Dr. med.

Role: primary

dominik.benz@usz.ch

+41 43 253 11 91

Mirjam Marty, MSc in Nursing

Role: backup

mirjam.marty@usz.ch

+41442552827

Other Identifiers

2024-02504

Identifier Type: -

Identifier Source: org_study_id