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A Study of Clinical Evaluation of a PET/MR System

Overview

Información sobre este estudio

The first objective of this pilot research protocol is to evaluate the quality of PET from the SIGNA PET/MR system and to compare the quantitative accuracy of PET images from the PET/MR system to PET images from a standard PET/CT system. The second objective of this pilot research protocol is to compare the image quality from MRI images acquired on the SIGNA PET/MR to clinical MR images acquired on a standard 3.0T MRI system.

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:

  • PET Cohort:
    • Patients 18 to 100 years of age
    • Patients who are scheduled for a clinically indicated F-18 FDG or Ga-68 DOTATATE PET/CT study
    • Patients who are able and willing to sign the informed consent will be enrolled
    • Patients who have a BMI of at least 18.5 kg/m²
    • Patients who pass standard clinical MRI screening procedures
  • MRI Cohort:
    • Patients 18 to 100 years of age
    • Patients who are able and willing to sign the informed consent will be enrolled
    • Patients who pass standard clinical MRI screening procedures
    • Patients who have had a clinical MRI scan performed within 7 days of the PET/MRI scan

Excluison Criteria:

  • PET Cohort
    • Patients who are unable to lay quietly for an additional 60 minutes of imaging
    • Patients who are claustrophobic
    • Patients who weigh more than 350 lbs or whose body habitus precludes them from participation
  • MRI Cohort:
    • Patients who are unable to lay quietly for an additional 60 minutes of imaging
    • Patients who are claustrophobic
    • Patients who weigh more than 350 lbs or whose body habitus precludes them from participation

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 Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Bradley Kemp, Ph.D.

Abierto para la inscripción

Contact information:

Kurt Kevin Degillo CCRP

(507)293-6682

Degillo.Kurt@mayo.edu

More information

Publicaciones

Publications are currently not available

Otros temas en investigación

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CLS-20308692

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