Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
700

Summary

Conditions
  • Cardiomyopathy, Dilated
  • Magnetic Resonance Imaging
  • Myocarditis
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

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 cardiologis...

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.

Tracking Information

NCT #
NCT02717143
Collaborators
Not Provided
Investigators
Principal Investigator: Phalla OU, MD. PhD Assistance Publique - Hôpitaux de Paris Principal Investigator: Claire BOULETI Assistance Publique - Hôpitaux de Paris