Skip to main content
Clinical Trials/NCT04844151
NCT04844151
Recruiting
N/A

Acute Myocarditis Registry With Prognostic, Histologic, Immunologic, Biological, Imaging and Clinical Assessment

Assistance Publique - Hôpitaux de Paris1 site in 1 country1,400 target enrollmentJanuary 23, 2022
ConditionsMyocarditis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Myocarditis
Sponsor
Assistance Publique - Hôpitaux de Paris
Enrollment
1400
Locations
1
Primary Endpoint
Major cardiac events
Status
Recruiting
Last Updated
11 months ago

Overview

Brief Summary

The AMPHIBIA study is an observational ambispective and prospective cohort that aim to describe the histologic, immunologic, biological, imaging, genetic and clinical characteristics of the patients hospitalized for an acute myocarditis and to evaluate their association with prognosis.

Detailed Description

Acute myocarditis is an inflammatory disease of the heart muscle. Its clinical presentation and its etiologies are multiple and make it a complex disease to treat. Its course also varies, ranging from complete clinical recovery to recurrence of ventricular arrhythmia or progression to chronic dilated heart disease, while being difficult to predict. The long-term prognosis is poorly understood. Consecutive patients hospitalized in a tertiary university referral center cohort from 2006 to 2041 for an acute myocarditis will be ambispectively or prospectively analyzed. This project will establish a registry including up to 400 patients in the ambispective analysis cohort from 2006 to 2021 and 1000 patients in the prospective analysis cohort during a 20 years inclusion period. The aim of the study is to describe the characteristics of patients hospitalized for an acute myocarditis and to evaluate their association wih the long term (until 20 years) prognosis. Features of interest will include : * Clinical * Biological * Etiological * Echocardiographic * Cardiac magnetic resonance imaging * Genetics (for the prospective cohort) * Anatomopathological The collection of clinical, biological and radiological data will represent an unique source allowing research teams in the coming years to access the data necessary to answer various specific questions (pathophysiological, diagnostic, prognostic) relevant to the state of knowledge on this pathology.

Registry
clinicaltrials.gov
Start Date
January 23, 2022
End Date
May 1, 2041
Last Updated
11 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Acute myocarditis confirmed by cardiac magnetic resonance according to Lake Louise modified criteria or by endomyocardial biopsy according to histologic, immunologic and immunohistochemic criteria.
  • affiliation to the French Health Care System "Sécurité sociale"

Exclusion Criteria

  • Severe valvulopathy
  • Complex congenital cardiopathy
  • Previous heart transplant
  • Known significative coronary disease

Outcomes

Primary Outcomes

Major cardiac events

Time Frame: up to 1 years

Defined as a composite of : * All cause death * Resuscitated cardiac arrest * Heart transplant * Longterm mechanical circulatory support * Ventricular arrhythmia after discharge * Hospitalization for heart failure * Hospitalization for myocarditis recurrence

Secondary Outcomes

  • Heart transplant(up to 20 years)
  • Major cardiac events(up to 20 years)
  • Resuscitated cardiac arrest(up to 20 years)
  • Longterm mechanical circulatory support(up to 20 years)
  • Supra ventricular arrythmia(up to 20 years)
  • All cause death(up to 20 years)
  • Cardiovascular death(up to 20 years)
  • Sustained ventricular arrhythmia after discharge(up to 20 years)
  • Hospitalization for myocarditis recurrence(up to 20 years)
  • Hospitalization for heart failure(up to 20 years)
  • Pericardial drainage(up to 20 years)
  • High grade atrioventricular block(up to 20 years)
  • Pericarditis(up to 20 years)
  • Left ventricular systolic function under 50%(up to 20 years)
  • Therapeutics during hospital stay(From the day of admission up to 90 days)

Study Sites (1)

Loading locations...

Similar Trials