A Study to Analyze Supine Breast MRI

Overview

Información sobre este estudio

The purpose of this study is to characterize the changes occurring in breast tumor-associated properties/ dimensions between the prone and supine imaging positions and to develop a dataset of supine-positioned MRIs that can be translated into an operative setting for real-time visualization.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Participants must be female.
  • Participants must have a pre-operative standard mammogram with or without ultrasound.
  • Participants must have biopsy confirmed and clinical stage I, stage II, or stage III non-inflammatory breast carcinoma (If biopsy was done at an outside hospital, pathology will be reviewed at MCR).
  • Patient must meet standard MRI guidelines and be able and willing to undergo MRI.
  • Participants will be restricted to those aged ≥18 and <80 years old.
  • Participants must understand the study and be willing to sign a written informed consent document.

Exclusion Criteria:

  • Participants with inflammatory breast cancer.
  • Participants who are pregnant and/or lactating.
  • Participants who are already enrolled in a conflicting investigational trial.
  • Participants with known active collagen vascular disease.
  • Participants with known implantable devices or breast implants.
  • Participants with prior history of ipsilateral breast carcinoma treated with BCS and radiation therapy.
  • Participants who are unable to undergo MRI because of documented contra-indications for contrast-enhanced MRI (including but not limited to renal failure).
  • Participants who exceed the weight limit for the operative surgical table, 350 lbs or who will not fit into the 60 cm diameter bore of the MRI scanner.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Robert Fazzio, M.D., Ph.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20460922

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