Creation of a National Multicenter Platform for the Study of Inflammatory Myocardial Disease: Pre-MYO Cohort

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorFundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia

About this trial

The objectives of this project are: 1) to comprehensively characterize a large national cohort of patients with suspected myocarditis, their clinical phenotype, care management, blood and imaging biomarkers, epidemiological, environmental and genetic data; 2) to retrospectively validate the accuracy of the new hsa-RNA-Chr8:96 biomarker for the diagnosis of myocarditis compared to conventional diagnosis; 3) to identify acquired and inherited mutations, and their interaction with the environment, which explain the susceptibility to myocarditis, its severity and response to treatment; 4) to study the lower incidence in women and the influence of age, considering socio-health and genetic factors.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Acute chest pain: pericardial or pseudo-ischemic.

Dyspnea on exertion or at rest for up to 3 months.

Dyspnea on exertion or at rest for 3 months - 1 year.

Unexplained palpitations / arrhythmias, sudden death recovered.

Disqualifiers

None

Trial population

All patients with clinical suspicion of myocarditis or inflammatory cardiomyopathy will be included, based on the presence of compatible clinical findings.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • characterization of a large national cohort of patients with suspected myocarditis or inflammatory cardiomyopathy.

    Other intervention

    characterization of a large national cohort of patients with suspected myocarditis or inflammatory cardiomyopathy.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

characterization of a large national cohort of patients with suspected myocarditis or inflammatory cardiomyopathy.

Subjects will be recruited during an emergency room visit or within their usual clinical practice among those patients who meet the criteria for participation in the study.

Time frame
Up to 3 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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