Clinical Evaluation and Deployment of a Clinical PET/MR System with a Data Registry

Overview

  • Study type

    Observational
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Jacksonville, Florida: 18-000322
    Sponsor Protocol Number: 18-000322

About this study

The purpose of this study is to assess and deploy a new PET/MR platform following the same quality control method as was done at other Mayo Clinic sites, i.e. Rochester and Arizona.

The secondary purpose is to initiate a data registry for the PET/MR studies allowing us to capture some basic information about the indications, findings, and relevant imaging and non-imaging biomarkers for the studies conducted. This will allow us to see trends in utilization as well as create preliminary data to inform future (IRB approved) investigations.

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. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria:

PET Cohort

  1. Patients 18 to 100 years of age
  2. Patients who are scheduled for a clinically indicated PET study
  3. Patients who are able and willing to sign the informed consent
  4. Patients who pass standard clinical MRI screening procedures

MRI Cohort

  1. Patients 18 to 100 years of age
  2. Patients who are able and willing to sign the informed consent
  3. Patients who pass standard clinical MRI screening procedures

Exclusion Criteria:

PET Cohort

  1. Patients who are unable to lay quietly for additional 60 minutes of imaging, after conclusion of clinical imaging exam
  2. Patients who are claustrophobic
  3. Pregnant and lactating women
  4. Patients whose body habitus precludes them from participation

MRI Cohort

  1. Patients who are unable to lay quietly for an additional 60 minutes of imaging, after conclusion of clinical imaging exam
  2. Patients who are claustrophobic
  3. Patients whose body habitus precludes them from participation

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Akash Sharma, M.D., M.B.A.

Contact us for the latest status

Contact information:

Akash Sharma M.D., M.B.A.

(904)953-2447

Sharma.Akash@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

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CLS-20424753

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