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Aortic Valve and Root Measurements Under Real-Time 3-Dimensional Visualization During Angiography

13 de julio de 2017 actualizado por: NYU Langone Health

The American College of Cardiology/American Heart Association guidelines place symptomatic severe Aortic Stenosis as a class I indication for aortic valve replacement. With the recently approved Edwards-Sapien TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high risk for open-heart surgery are now eligible to undergo TAVR.

Patients selected for TAVR undergo an EKG-gated cardiac Multislice CTA to evaluate aortic valve anatomy and aortic root dimensions for device sizing, as well as coronary angiography to define coronary anatomy. Both tests utilize contrast media to visualize anatomy, which may result in contrast-induced nephropathy in anywhere from 7.5% to more than 50% of patients depending on associated clinical risk factors.

There is a need to consolidate this pre-operative testing whenever possible, and with real-time 3-dimensional visualization of aortic valve and root anatomy using DynaCT cardiac acquisition in the cath lab angiography suite during the coronary angiography, there may be a benefit with reduced contrast load (20 to 35cc for DynaCT, 100cc for CTA).

We would like to make a comparison of aortic valve and root measurements using CTA and DynaCT to affirm the accuracy of DynaCT vs the CTA gold standard.

Descripción general del estudio

Descripción detallada

Calcific or degenerative aortic valve disease is one of the most common valvular diseases among the elderly and, with life expectancy continuing to increase, a major source of burden on current healthcare. Although patients with aortic stenosis (AS) can remain asymptomatic for a prolonged period, they do eventually develop symptoms, including angina, exertional syncope and heart failure, which is associated with a 5-year, 3-year, and 1-year, respectively, 50% mortality. The American College of Cardiology/American Heart Association guidelines place symptomatic severe AS as a class I indication for aortic valve replacement. Currently, surgical replacement of the aortic valve is the standard of care. However, with the recently approved Edwards-Sapient TAVR device and the ongoing investigations using the CoreValve TAVR device, patients ineligible or at high risk for open-heart surgery are now eligible to undergo TAVR.

Currently, patients selected for TAVR undergo an EKG-gated cardiac Multislice CTA to evaluate aortic valve anatomy and aortic root dimensions for device sizing. Patients also undergo coronary angiography to define coronary anatomy. Both tests utilize contrast media to visualize anatomy, which may result in contrast-induced nephropathy in anywhere from 7.5% to more than 50% of patients depending on associated clinical risk factors. Contrast-induced nephropathy can, in turn, lead to dialysis and/or increased mortality.

There is a need to consolidate this pre-operative testing whenever possible, and with real-time 3-dimensional visualization of aortic valve and root anatomy using DynaCT cardiac acquisition in the cath lab angiography suite during the coronary angiography, there may be a benefit with reduced contrast load (20 to 35cc for DynaCT, 100cc for CTA). DynaCT conducts fully automatic aortic root segmentation and overlays 3-dimensional structures onto 2-dimensional fluoroscopy in a few seconds (~5 seconds, 60 frames/second rotational angiography). The software automatically recognizes and represents the aortic root, detects and indicates coronary ostia and lowest cusp points of aortic valve (nadir points), and reconstructs commissure lines of aortic valve. Due to cardiac motion, 3-dimensional images without motion correction or cardiac gating will look blurred. Therefore, DynaCT reconstruction motion correction software will be used. The DynaCT motion correction software is a new algorithm that will correct for this motion and apply it during reconstruction- allowing the user to spin without using rapid pacing. However, first, a comparison of aortic valve and root measurements using CTA and DynaCT must be made to affirm the accuracy of DynaCT vs the CTA gold standard.

Study Design This is a pilot study evaluating patients undergoing TAVR at the New York University (NYU) Langone Medical Center. Patients will undergo the standard CTA protocol and invasive coronary angiography performed as part of the pre-operative assessment for TAVR. However, patients in this study will also undergo DynaCT during coronary angiography, utilizing 1 acquisition sweep and 20 to 35cc more of contrast media. Measurements of the major aortic annulus diameter, orthogonal minor aortic annulus diameter, aortic annulus perimeter, maximum ascending aorta diameter at 40mm above the annulus, sinus of Valsalva diameters, sinus of Valsalva heights, and aortic root angulation will be made using both the CTA and DynaCT protocols by a radiologist blinded to patient identity after the study has reached its target recruitment. Based on these measurements, a trained interventional cardiologist will select the appropriate TAVR size in a similarly blinded fashion after the study has reached its target recruitment (i.e. the data collected using DynaCT will not be used in the clinical decision making process). Data will be compared from both modalities using appropriate tests of reproducibility and correlation.

Study Technique CTA will be performed per standard methods as part of standard pre-TAVR evaluation.

Coronary angiography will be performed via femoral artery access (minimum 6Fr) as per standard pre-TAVR evaluation. After coronary angiography is performed, a 6Fr pigtail catheter will be placed in the aorta and 40cc of 50% contrast media diluted normal saline will be delivered using standard automated injection during dynaCT cardiac image acquisition. Intravenous delivery of contrast was considered as alternative.

As per standard care, intravenous access will be obtained and participants will be hydrated during the CTA, coronary angiography, and dynaCT procedures.

Tipo de estudio

Intervencionista

Inscripción (Actual)

25

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

    • New York
      • New York, New York, Estados Unidos, 10016
        • NYU Langone Medical Center

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:

  • Subjects must be more than 18 years of age with a plan to undergo TAVR.

Exclusion Criteria:

  • Subjects will be excluded if they meet one of the following criteria:

    1. estimated glomerular filtration rate <40 mL/min/1.73m2;
    2. highly irregular heart rates, frequent extra systoles, additional extra pulsations, not in sinus heart rhythm;
    3. allergy to contrast media;
    4. pregnant; or
    5. Unable to consent.

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: Real-time 3-dimensional DynaCT
Patients will undergo the standard CTA protocol and invasive coronary angiography performed as part of the pre-operative assessment for TAVR. Patients in this study will also undergo DynaCT during coronary angiography, utilizing 1 acquisition sweep and 20 to 35cc more of contrast media. Measurements of the major aortic annulus diameter, orthogonal minor aortic annulus diameter, aortic annulus perimeter, maximum ascending aorta diameter at 40mm above the annulus, sinus of Valsalva diameters, sinus of Valsalva heights, and aortic root angulation will be made using both the CTA and DynaCT protocols by a radiologist blinded to patient identity. Based on these measurements, a trained interventional cardiologist will select the appropriate TAVR size for the patient.
After coronary angiography is performed, a 6Fr pigtail catheter will be placed in the aorta and 40cc of 50% contrast media diluted normal saline will be delivered using standard automated injection during dynaCT cardiac image acquisition. Intravenous delivery of contrast as alternative.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Correlation of aortic annulus measurement measured on invasive 3D dyna CT (experimental) and on non-invasive CT scan (standard of care)
Periodo de tiempo: 1 day
Each patient will undergo non-invasive CT scan for aortic annulus measurement (in order to choose appropriate TAVR size) as per standard of care. They will then undergo invasive dyna CT for aortic annulus measurement during their clinically-indicated invasive coronary angiogram. The primary outcome is correlation between the aortic annulus dimension measurement made on dyna CT and non-invasive CT.
1 day

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
TAVR size
Periodo de tiempo: 1 day
A trained interventional cardiologist will evaluate the measurements made from each CTA abd DynaCT image and select the appropriate TAVR size in a blinded fashion.
1 day

Colaboradores e Investigadores

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

Patrocinador

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)

6 de enero de 2014

Finalización primaria (Actual)

22 de junio de 2016

Finalización del estudio (Actual)

13 de junio de 2017

Fechas de registro del estudio

Enviado por primera vez

19 de febrero de 2014

Primero enviado que cumplió con los criterios de control de calidad

26 de febrero de 2014

Publicado por primera vez (Estimar)

27 de febrero de 2014

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de julio de 2017

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

13 de julio de 2017

Última verificación

1 de julio de 2017

Más información

Términos relacionados con este estudio

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

producto fabricado y exportado desde los EE. UU.

No

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