Diagnostic Utility of F-18 Florbetapir PET/MR in Peripheral Nerve Amyloidosis



Status:Enrolling by invitation
Conditions:Hematology
Therapuetic Areas:Hematology
Healthy:No
Age Range:18 - 100
Updated:8/15/2018
Start Date:March 13, 2017
End Date:December 2020

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The primary aim of this study will be to examine the diagnostic utility of 18-F Florbetapir
PET/MR (Positron Emission Tomography/Magnetic Resonance) in imaging patients with
pathologically-confirmed systemic amyloidosis involving the peripheral nerves and compare
these results to non-amyloid diseased controls.

Patients with pathologically proven amyloidosis involving the peripheral nervous system will
undergo 18-F Florbetapir PET/MR on a GE (General Electric Healthcare) SIGNA PET/MR scanner. A
control arm comprised of patients with pathologically-confirmed non-amyloid causes of
peripheral neuropathy will also undergo 18-F Florbetapir PET/MR scanning. all images will be
reviewed for peripheral nerve uptake.

Inclusion Criteria:

- Adults: 18-100

- Pathologically-confirmed peripheral nerve amyloidosis or pathologically-confirmed
non-amyloid causes of peripheral neuropathy

Exclusion Criteria:

- Metallic devices that are not MR safe (cardiac pacers, stents, aneurysm coils, etc.)

- Claustrophobia

- BMI over 38
We found this trial at
1
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200 First Street SW
Rochester, Minnesota 55905
507-284-2511
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