Observational Epidemiological Study of Patients Suffering From Systemic Amyloidosis

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna

About this trial

observational epidemiological study of patients affected by systemic amyloidosis

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients diagnosed with amyloidosis or asymptomatic carriers of mutations in the transthyretin gene

minimum age of 18 years at the time of diagnosis

obtaining informed consent

Disqualifiers

nothing

Trial population

The study population includes all adult patients referred to the participating centers with a diagnosis of amyloidosis or carriers of pathogenic mutations starting from 01/01/1981 diagnosed in accordance with current international guidelines.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

prevalence of amyloidosis

prevalence of amyloidosis in patients admitted to the UOs participating in the study

Time frame
throughout the study period until 10 years
2

incidence of amyloidosis

incidence of amyloidosis in patients admitted to the UOs participating in the study

Time frame
throughout the study period until 10 years
3

Observational epidemiological study of patients with systemic amyloidosis

characteristics of each etiology in terms of baseline clinical data

Time frame
throughout the study period until 10 years
4

Types of cardiac clinical phenotype

Cardiac clinical phenotype in patients who at baseline are asymptomatic carriers of pathogenic mutations

Time frame
throughout the study period until 10 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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