French Registry of CMR Late Gadolinium Enhancement in Myocarditis

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

Acute myocarditis is a major cause of death in young adults and carries substantial morbidity, including a significant risk of progression to dilated cardiomyopathy. Current diagnostic and therapeutic strategies remain poorly defined, making risk stratification crucial to enable personalized treatments and reduce mortality and major cardiovascular events.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

Ability to provide informed non-opposition

AM diagnosis confirmed using CMR, fulfilling the modified Lake Louise diagnostic criteria

Disqualifiers

None

Trial population

The study will include all consecutive patients with AM referred for CMR assessment.

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

All-cause mortality

All-cause mortality defined using the French national registry of death (INSEE).

Time frame
From enrollment to the end of follow up at 10 years

Secondary outcomes

1

All-cause death

Time frame
From enrollment to the end of follow up at 10 years
2

Heart transplantation

Time frame
From enrollment to the end of follow up at 10 years
3

Ventricular arrhythmia

Time frame
From enrollment to the end of follow up at 10 years
4

Hospitalisation for acute heart failure

Time frame
From enrollment to the end of follow up at 10 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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