degenerative joint disease, Osteoarthritis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Age >= 18 yrs - Scheduled to undergo primary total shoulder arthroplasty (TSA) or reversed shoulder arthroplasty (RSA) for primary shoulder osteoarthritis or cuff tear arthropathy - American Society of Anesthesiologists score 1, 2 or 3 - Able to provide written informed consent
Exclusion criteria
Exclusion criteria: - Regular use of anti-depressants or anti-epileptics for any purpose, including SNRIs and gabapentinoids - The presence of any chronic pain disorder other than osteoarthritis - Osteoarthritis in joints other than the affected shoulder, for which arthroplasty is/will be planned in the near future • Difficulty with or inability to perform psychophysical testing (eg. in case of cognitive or psychiatric disorders) - Difficulty with or inability to communicate with the investigators (eg. difficulty with the Dutch language, cognitive/memory disorders)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main study parameters are CPM and TS values at baseline and at 3 and 6 months after surgery, as well as the absence/presence of allodynia at baseline and at 3 and 6 months after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are painscores, pain catastrophizing and coping strategies at baseline and at 3 and 6 months after surgery. | — |
Countries
Netherlands
Contacts
Reinier Haga Orthopedisch Centrum