Actively Recruiting

Age: 18Years +
All Genders
ID04776824

Swiss Cardiac Amyloidosis Registry (Swiss-CARE) Observational Study

Led by Insel Gruppe AG, University Hospital Bern · Updated on 2025-05-06

300

Participants Needed

7

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Cardiac transthyretin amyloidosis (ATTR) is a condition where misfolded transthyretin protein deposits in the heart, causing thickening of the heart walls and leading to heart dysfunction and failure. Researchers are investigating imaging markers using cardiac magnetic resonance (CMR) techniques like feature tracking and T1- and T2-mapping to better understand disease severity and identify patients who may benefit from treatment that stabilizes transthyretin. The study collects detailed CMR imaging data from patients with amyloidosis, including measures of heart function and tissue characteristics, over an 18-month period after therapy begins. Clinical and laboratory follow-up visits occur every 3 to 6 months. This observational research gathers retrospective and prospective data from patients diagnosed at a single hospital to evaluate how these imaging markers relate to disease progression and treatment response. Participants undergo regular assessments including CMR scans to measure left and right ventricle function, tissue changes, and extracellular volume. The study aims to use these imaging results to predict major adverse cardiac events over a five-year period. Researchers will also monitor clinical status and laboratory values during follow-up visits to better understand the impact of treatment and disease progression.

CONDITIONS

Brief Title

Swiss Cardiac Amyloidosis REgistry (Swiss-CARE)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Confirmed diagnosis of amyloidosis with or without cardiac involvement
  • Provided general consent to participate
Not Eligible

You will not qualify if you...

  • Unable to give consent or has refused data use in writing or orally
  • Under 18 years of age

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Baseline assessment

Participants undergo cardiac magnetic resonance imaging (CMR) and clinical assessments to evaluate cardiac amyloidosis and establish baseline measures.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 18 months

Participants are monitored with clinical and laboratory follow-up every 3 to 6 months and repeated CMR assessments over 18 months to track disease progression and therapy response.

Follow-up visits every 3 to 6 months

Trial Site Locations

Total: 7 locations

1

USB

Basel, Switzerland, 4031

Not Yet Recruiting

2

Department of Cardiology, University Hospital Bern, Inselspital, Bern

Bern, Switzerland, 3010

Actively Recruiting

3

HUG

Geneva, Switzerland, 1211

Actively Recruiting

4

CHUV

Lausanne, Switzerland, 1011

Actively Recruiting

5

LUKS

Lucerne, Switzerland, 6000

Actively Recruiting

6

KSSG

Sankt Gallen, Switzerland, 9007

Actively Recruiting

7

Stadtspital Triemli

Zurich, Switzerland, 8063

Actively Recruiting

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Research Team

C

Christoph Gräni, MD, PhD

M

Moritz Hundertmark, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Frequently Asked Questions

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Published Research Related To This Trial

Correlation of global and regional quantitative 99m Tc-3,3-diphosphono-1,2 propanodicarboxylicacid single-photon emission computed tomography with echocardiography in patients with suspected transthyretin-related cardiomyopathy.

Federico Caobelli, Cristina E Popescu, Nasir Gözlügöl...

https://pubmed.ncbi.nlm.nih.gov/41804669

Prognostic Value of [99mTc]Tc-DPD Quantitative SPECT/CT in Patients with Suspected and Confirmed Amyloid Transthyretin-Related Cardiomyopathy and Preserved Left Ventricular Function.

Federico Caobelli, Nasir Gözlügöl, Adam Bakula...

https://pubmed.ncbi.nlm.nih.gov/38724281