R52.2
Conditions
Interventions
Group 1: The aim of this study is to determine the endocannabinoid- and immune system in patients with chronic pain. All patients will receive study-independent standard treatment of the corresponding
Sponsors
Interdisziplinäre Schmerzambulanz und Tageskinik, LMU München, Klinikum Großhadern
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patients with chronic nociceptive and/or neuropathic pain without medication or stable medication for at least 14 days
Exclusion criteria
Exclusion criteria: Pregnancy, psychological/mental disorder, addiction, glucocorticoid treatment
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Before and after standard treatment: Pain level: NRS, Stresslevel: KAB, Cytokines: Immunassay, Endocannabinoids: Mass-spektrometry, T cells: Flow cytometry, mRNA-expression: RT-PCR | — |
Secondary
| Measure | Time frame |
|---|---|
| Influences of routine standard pain treatment on the primary outcome parameters. | — |
Countries
Germany
Contacts
Public ContactShahnaz Christina Azad
Interdisziplinäre Schmerzambulanz und Tageskinik, LMU München, Klinikum Großhadern
Outcome results
None listed