Amyloidosis
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Patients aged 18 years or older who have been definitively diagnosed with amyloidosis 2.Patients who are able to express their will and have voluntarily agreed to participate in the study, or patients who are unable to express their will and have their proxy consent to participate in the study
Exclusion criteria
Exclusion criteria: 1.Patients with a history of allergies to the study drug 2.Other subjects who the principal investigator deems inappropriate to be subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The intensity and pattern of cardiac accumulation of two types of tracers (99mTc-HMDP and 18F-Flutemetamol), the relationship between the intensity and clinical parameters, and the time course of the accumulation if positive. | — |
Secondary
| Measure | Time frame |
|---|---|
| Detectability of amyloid deposits in organs other than the heart using two imaging methods | — |
Countries
Japan
Contacts
Shinshu University School of Medicine Department of Medicine (Neurology and Rheumatology)