MYOCARDITIRM: French National Observatory Tracking Viral Myocarditis: Mortality, Cardiovascular Events, Sequels on (Magnetic Resonance Imaging) MRI

Sponsor
French Cardiology Society (Other)
Overall Status
Unknown status
CT.gov ID
NCT02717143
Collaborator
(none)
821
1
68
12.1

Study Details

Study Description

Brief Summary

Acute myocarditis is a serious illness affecting a young population with a very variable course (of full recovery at the onset of dilated cardiomyopathy (DCM), or even sudden death). Very few studies have examined the predictors of death and serious cardiovascular events in acute myocarditis and have carried on numbers of restricted patients. What little data results in a lack of a precise recommendation on the management and the follow-up period of patients.

This observational study should identify serious prognostic factor for cardiovascular events in order to provide a support strategy and more appropriate monitoring of myocarditis.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Patients included in the study benefit from clinical monitoring, ultrasound and MRI as planned according to the habits of the center, regardless of the study. These clinical monitoring data, ultrasound and MRI will be collected as part of the study and if necessary telephone follow-up of cardiologists contractors will be made to complete the data. No additional examination will be conducted as part of this study. The data collected especially for cardiac MRI, will be based on the current monitoring protocol in each center.

    All patients included in this study have received information and signed a consent to the use of their data during hospitalization and follow-up.

    As part of this study, the inclusions are planned for a period of 2 years or more to reach a recruitment of 700 patients. The tracking target is 3 years, with an annual follow-up.

    Patient follow-up is made by the doctor who selected the patient. Clinical follow-up will be made at a consultation normally provided for in hospital or cardiology practice in this type of pathology.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    821 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    French National Observatory Tracking Viral Myocarditis: Mortality, Cardiovascular Events, Sequels on (Magnetic Resonance Imaging) MRI
    Actual Study Start Date :
    Apr 1, 2016
    Anticipated Primary Completion Date :
    Apr 1, 2021
    Anticipated Study Completion Date :
    Dec 1, 2021

    Arms and Interventions

    Arm Intervention/Treatment
    Acute myocarditis

    Patients with a clinical picture suggestive of acute myocarditis: increase of troponin above the threshold defined by the pathological laboratory, associated with at least one of the three following criteria: prolonged chest pain > 10 minutes, recent infectious context <7 days young subject and / or absence of cardiovascular risk factors and / or absence of significant coronary lesion Patients will be included after completion of MRI confirm the diagnosis. They will be followed for 3 years, every year, by the doctor who included them in the study. This is an observational study that does not affect the management of patients.

    Outcome Measures

    Primary Outcome Measures

    1. All cause mortality at 1 year of follow-up [1 year]

    2. Cardiovascular mortality at 1 year of follow-up [1 year]

    Secondary Outcome Measures

    1. All cause mortality at 3 years of follow-up [3 years]

    2. Incidence of cardiovascular events at 3 years of follow-up [3 years]

      Incidence of heart failure requiring hospitalization, diagnostic of DCM not posed before the episode of myocarditis, stroke, heart transplant

    3. Incidence of sequelae of myocarditis in cardiac MRI for patients undergoing cardiac MRI in their monitoring at 3 years of follow-up [3 years]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Patient aged 18 years and over

    • Hospitalized suspect table of acute myocarditis: Eligible patients must have an increase of troponin I greater than the threshold value of the pathological laboratory of Biochemistry, associated with at least one of the three following criteria:

    1. prolonged chest pain> 10 minutes,

    2. recent infectious context <7 days

    3. subject young and / or absence of cardiovascular risk factors and / or absence of significant coronary lesions in coronary angiography if the patient had a coronary angiography.

    • Having received a cardiac MRI which concluded the diagnosis of acute myocarditis according to the usual criteria of the center (Lake Louise criteria changed according to the habits of the center) There myocarditis when at least two of the following criteria are met: hyperintense T2; hyperintense Diffusion; myocardium ratio signal / peripheral muscle Gadolinium> 4; contrast enhancement after injection of gadolinium chelate in cine-steady-state free precession (SSFP); nonischemic type of signal on delayed enhancement. These anomalies are segmental topography typically subepicardial. The analysis is made of the 17 segments of the left ventricle.

    • Patient was informed and has given its consent for the study

    Exclusion Criteria:
    • Refusal of consent

    • Claustrophobia

    • Formal contraindications to MRI (allergic reaction to gadolinium chelates, porters pregnancy or patients against-indicated materials listed on the site MRI Safety "www.MRIsafety.com") :

    • Incompatible heart Pacemaker and Defibrillator

    • heart valve prostheses: valves Starr

    • Metal splinters

    • Coils intra cranial, intra cerebral surgical clips, bypass valves

    • Neurological stimulators

    • Insulin Pumps

    • Orthopedic Materials: cervical fixation with cervical Halo vest or fixer

    • Body piercing not be withdrawn

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Bichat Paris France

    Sponsors and Collaborators

    • French Cardiology Society

    Investigators

    • Principal Investigator: Phalla OU, MD. PhD, Assistance Publique - Hôpitaux de Paris
    • Principal Investigator: Claire BOULETI, Assistance Publique - Hôpitaux de Paris

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    French Cardiology Society
    ClinicalTrials.gov Identifier:
    NCT02717143
    Other Study ID Numbers:
    • 15677
    First Posted:
    Mar 23, 2016
    Last Update Posted:
    Aug 7, 2019
    Last Verified:
    Aug 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Keywords provided by French Cardiology Society
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 7, 2019