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Predicción de la remodelación inversa y el resultado en pacientes con insuficiencia valvular mitral secundaria grave que se someten a una reparación percutánea de la válvula mitral de borde a borde (PRE-MITRA)

5 de noviembre de 2026 actualizado por: Insel Gruppe AG, University Hospital Bern

The investigators' hypothesis is that CMR tissue characterization and myocardial function analysis acquired by CMR feature tracking technique predict reverse remodeling in patients with severe secondary mitral regurgitation (MR) undergoing transcatheter mitral edge-to-edge repair.

Descripción general del estudio

Descripción detallada

Diametrically opposed results of the COAPT- and the MITRA-FR trial have demonstrated the need for additional evidence in the field of transcatheter mitral edge-to-edge repair. Reverse left ventricular remodeling after treatment of severe secondary mitral regurgitation can indicate treatment response and is associated with positive outcomes.

However, so far it is reverse remodeling, respectively treatment response is difficult to predict, which complicates patient selection for mitral edge-to-edge repair. Previous studies have shown, that focal (late gadolinium enhancement (LGE)) but not diffuse myocardial fibrosis (T1 mapping and extracellular volume fraction (ECV)) burden quantification using CMR predicts reverse left ventricular remodeling following cardiac resynchronization therapy in patients with heart failure with reduced ejection fraction (HFrEF). On the other hand, myocardial T1 mapping was predictive for beneficial left ventricular remodeling after long-term heart failure therapy. Furthermore, in patients with HFrEF, LGE is associated with clinical outcome and an incremental predictive value to left ventricular dimensions and function. However, as only 1/3 of HFrEF patients show LGE, subtle fibrosis might be missed. Recently the investigators have shown that different novel fibrosis detection techniques (naive T1 mapping, mean ECV and λGd being the delta of pre- and post T1 mapping and ECV calculation) all demonstrated strong association with outcome in patients with heart failure.

The investigators' hypothesis is that these markers (CMR tissue characterization and myocardial function analysis acquired by a CMR feature tracking) might also be helpful in predicting reverse remodeling after transcatheter mitral edge-to-edge repair. This project might help to understand the pathophysiology of the disease in patients with secondary mitral regurgitation, improve risk stratification in this clinical setting, and optimize selection of patients who benefit from transcatheter mitral edge-to-edge repair.

Tipo de estudio

Intervencionista

Inscripción (Actual)

39

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Bern, Suiza, 3010
        • Department of Cardiology, University Hospital Bern, Inselspital, Bern

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Patients with severe secondary MR characterized, according to the European guidelines and recommendations, by a regurgitant volume ≥30 mL/beat or an effective regurgitant orifice ≥20 mm².
  • Symptomatic patients with New York Heart Association Class ≥II.
  • Left ventricular ejection fraction between 15% and 50%.
  • Optimal standard of care therapy for heart failure according to investigator.
  • Not eligible for a mitral surgery intervention according to the Heart Team.
  • Patients who have the ability to understand the requirements of the study and provide written consent/assent to participate and agree to abide by the study requirements.

Exclusion Criteria:

  • Participants younger than 18 years
  • Pregnancy or breastfeeding
  • Severe impaired renal function (GFR < 15 ml/min)
  • Patients with untreated severe concomitant valve disease (e.g. severe tricuspid valve regurgitation, aortic stenosis)
  • The patient has a medical condition, serious concurrent illness, or extenuating circumstance that would significantly decrease study compliance, including all prescribed follow-up
  • The patient has contraindications to CMR, including: Implanted non-CMR conditional metallic implants, pacemaker, intracardiac defibrillator, neurostimulator, epicardial pacemaker leads, or any abandoned leads, ferromagnetic aneurysm clip, ferromagnetic halo device, cochlear implants, implanted infusion pumps or severe claustrophobia
  • The patient is clinically unstable or has stage D congestive heart failure or inability to lay flat for 60 minutes

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Diagnóstico
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment Arm

Patients undergoing transcatheter mitral edge-to-edge repair in this single-arm study.

CMR image acquisition with previously mentioned analysis

Included patients will undergo Transcatheter mitral edge-to-edge repair.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Rate of patients with reverse remodeling after 12 months
Periodo de tiempo: 12 months after mitral edge-to-edge repair

Defined as ≥10% reduction in left ventricular end-diastolic volume in patients with successful MR reduction to grade 2+ or less 12 months after mitral edge-to-edge repair assessed by echocardiography.

12 months after mitral edge-to-edge repair

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Rate of patients with procedural and device success
Periodo de tiempo: 24 months after mitral edge-to-edge repair

Procedural and device success as defined according to the criteria of the Mitral Valve Academic Research Consortium

24 months after mitral edge-to-edge repair
Rate of patients with reverse remodeling after 6 and 24 months
Periodo de tiempo: 6 and 24 months after mitral edge-to-edge repair

Reverse remodeling at 6 and 24 months, defined according to previously mentioned criteria.

6 and 24 months after mitral edge-to-edge repair
Change of left ventricular sphericity index
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Echocardiographic assessment of LV sphericity index measured using the LV short/long axis dimension ratio in the end-diastolic four-chamber apical view.

6, 12 and 24 months after mitral edge-to-edge repair
Change in NT-proBNP levels
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Change in NT-proBNP levels as an indirect sign of changes in left ventricular filling pressure, fibrosis and reverse remodeling will be measured in clinically indicated follow-ups at different time points after the intervention.

6, 12 and 24 months after mitral edge-to-edge repair
All cause death
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Occurence of death from any cause

6, 12 and 24 months after mitral edge-to-edge repair
Cardiovascular death
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Occurence of death from cardiovascular reason

6, 12 and 24 months after mitral edge-to-edge repair
Rate of patients with heart-failure related hospitalization
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Hospitalizations for heart failure within the observation time will be systematically recorded.

6, 12 and 24 months after mitral edge-to-edge repair
Change in NYHA class
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Change in NYHA class ≥ +/- 1 compared to baseline NYHA-class before mitral edge-to-edge repair.

6, 12 and 24 months after mitral edge-to-edge repair
Change in myocardial strain
Periodo de tiempo: Within 24 months after mitral edge-to-edge repair

Clinically indicated follow-up imaging (CMR) will be analyzed by CMR feature tracking

Within 24 months after mitral edge-to-edge repair
Change in left ventricular ejection fraction
Periodo de tiempo: 6, 12 and 24 months after mitral edge-to-edge repair

Echocardiographic assessment of left ventricular ejection fraction measured according to biplane Simpson disk summation method.

6, 12 and 24 months after mitral edge-to-edge repair

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Christoph MD Gräni, PHD, Department of Cardiology, University Hospital Bern, Inselspital, Bern

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

4 de agosto de 2021

Finalización primaria (Actual)

28 de febrero de 2025

Finalización del estudio (Actual)

30 de septiembre de 2026

Fechas de registro del estudio

Enviado por primera vez

27 de mayo de 2021

Primero enviado que cumplió con los criterios de control de calidad

3 de junio de 2021

Publicado por primera vez (Actual)

4 de junio de 2021

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

5 de noviembre de 2026

Última verificación

1 de diciembre de 2025

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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