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Clinical Trials in Italy / NCT06799273
Recruiting Observational

MECKI-Amyloidosis: Assessment of the Exercise Capacity and Prognosis of Patients with Cardiac Amyloidosis

NCT06799273 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2024-05-07
Last updated
2025-01-29

Condition(s) studied

Cardiac Amyloidosis

Study summary

This study aims to advance the understanding of cardiac amyloidosis, its effects on exercise capacity, and its prognostic implications. By conducting a systematic investigation with particular emphasis on longitudinal evaluation, we aim to provide valuable insights to guide clinical practice and improve the management of patients with cardiac amyloidosis.

Our study intends to follow patients for a period of two years, evaluating them every six months. This longitudinal approach allows us to monitor changes in exercise capacity and other relevant clinical parameters over time. Furthermore, it enables the development of a prognostic tool similar to the MECKI score, capable of assessing the risk of adverse events in patients with cardiac amyloidosis based on their exercise performance.

By comparing our results with data from heart failure patients already included in the MECKI score database, we also aim to highlight any differences in prognosis between patients with cardiac amyloidosis and those with general heart failure. Finally, we aim to characterize cardiac amyloidosis by differentiating it from general heart failure. By comparing our results with data from heart failure patients already included in the MECKI score database, we can clarify the distinct exercise limitations in cardiac amyloidosis and shed light on how they differ from more conventional heart failure.

Eligibility

Sex
ALL
Min age
18 Years
Max age
100 Years
Healthy volunteers
No
Inclusion criteria * Age \> 18 years * Diagnosis of cardiac amyloidosis obtained by MRI or scintigraphy * Ability to perform a cardiopulmonary exercise test Exclusion criteria * severe obstructive pulmonary disease * exercise-induced angina * significant ECG changes * presence of clinical comorbidities that interfere with exercise performance

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centro Cardiologico Monzino, Irccs Milan Italy Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06799273 on ClinicalTrials.gov ↗ ← All trials in Italy