M54 G43
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) Age: 18 - 80 (2) voluntary, informed study participation (3) chronic low back pain or chronic migraine (> 3 months; for migraine: attacks on > 15 days per month); healthy control subjects (matched to pain patients in age, gender, education)
Exclusion criteria
Exclusion criteria: (4) participation in other clinical trials testing medication (5) severe depression or anxiety disorder (6) pregnancy, nursing (7) medication-overuse headache (MOH) (8) other chronic pain conditions except lower back pain or migraine (esp. radicular pain, neuropathic pain) (9) intake of highly dosed opioids (10) contraindication for MR testing, e.g. • cardiac pacemaker and other magnetizable material within the body • MR-incompatible metal material • claustrophobia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| mean reaction times (ms) (categorisation task) and recognition performance (d prime, recollection and familiarity parameters) for images previously presented with electrical pain stimuli (1) at the lower back (L3-L5), (2) at the forehead (V1) or (3) without additional painful stimulation; Group comparison: (1) patients suffering from chronic lower back pain, (2) patients suffering from chronic migraine and (3) healthy control subjects. interaction effects: group x condition | — |
Secondary
| Measure | Time frame |
|---|---|
| 1) mean skin conductance response (amplitude, microsiemens; latency, ms) during painful stimulation and during the recognition task (for each experimental phase: main effect group, main effect stimulation, interaction group x stimulation) 2) Structural and functional predispositions (morphometry, resting state fMRI) | — |
Countries
Germany
Contacts
Universitätsklinik Essen AöR; Klinik für Neurologie