R52.9
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Diabetes mellitus-induced neuropathic pain 1. capable of giving consent 2. age = 50 years 3. diabetes mellitus 4. neuropathic pain Cancer chemotherapy-induced neuropathy pain 1. capable of giving consent 2. age = 50 years 3. neuropathic pain 4. group after chemotherapy Nerve injury-induced neuropathic pain 1. capable of giving consent 2. age = 50 years 3. neuropathic pain after nerve injury Reactive/inflammation-induced visceral pain 1. capable of giving consent 2. age = 50 years 3. visceral pain of reactive or inflammatory origin inflammatory arthrosis 1. capable of giving consent 2. age = years 3. inflammatory arthrosis 4. pain as a result of inflammatory arthrosis
Exclusion criteria
Exclusion criteria: Diabetes mellitus-induced neuropathic pain 1. any radiation exposure for scientific purposes within the last 10 years. Cancer chemotherapy-induced neuropathy pain 1. any radiation exposure for scientific purposes within the last 10 years. Nerve injury-induced neuropathic pain 1. any radiation exposure for scientific purposes within the last 10 years. Reactive/inflammation-induced visceral pain 1. any radiation exposure for scientific purposes within the last 10 years. inflammatory arthrosis 1. any radiation exposure for scientific purposes within the last 10 years.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Signal intensity and segmental extension of the PSMA tracer over a period of 1-3 hours after tracer injection in relation to reference regions such as musculature | — |
Secondary
| Measure | Time frame |
|---|---|
| - Signal intensity of the PSMA tracer in reference regions (e.g. salivary glands, blood pool, liver, spleen and muscles) - Time course of PSMA PET signal intensity in reference regions (e.g. salivary glands, blood pool, liver, spleen and muscles) - Comparison of PSMA PET signal intensity in different pain conditions | — |
Countries
Germany
Contacts
Klinik und Poliklinik für Nuklearmedizin