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A Study of Advanced Magnetic Resonance Technology Design Toward Enhancing Its Value

Overview

About this study

The purpose of this study is to develop and test a wide range of software, all designed to operate an MRI scanner more efficiently - to produce higher quality images, with less undesired variability, in a shorter exam time and with a better patient experience.
 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Adult male and non-pregnant female subject is at least 18 years of age.
  • Subjects who are MRI compatible and pass the clinical MRI screening procedures.
  • Subject is willing and capable of providing informed consent and participating in this trial.

Exclusion Criteria:

  • Subjects who have a contraindication to MRI scanning such as a cardiac pacemaker, claustrophobia, the presence of intraocular or intracranial metallic objects, and all other devices that are incompatible with MRI.
  • Subjects who are claustrophobic.
  • Subjects who weigh more than 350 pounds or who body habitus preclude them from participation.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Tim Leiner, M.D., Ph.D.

Open for enrollment

Contact information:

James Pipe Ph.D.

(507) 293-9363

Pipe.James@mayo.edu

More information

Publications

Publications are currently not available

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CLS-20506964

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