Preoperative pain treatment by means of duloxetine will improve postoperative outcome after total hip or knee arthroplasty by reducing residual pain
ID
Bron
Verkorte titel
Aandoening
osteoarthritis; central sensitization; peripheral sensitization; residual pain
Dutch: artrose; centrale sensitisatie; perifere sensitisatie; residuele pijn
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Degree of pain relief 6 months after total hip or knee arthroplasty
Achtergrond van het onderzoek
Total Joint Replacement is considered a successful treatment for end stage osteoarthritis. However, residual pain after Total Joint Replacement forms a substantial problem affecting up to 23% - 34% of patients after Total Hip or Knee Replacement (THR/TKR). There is a growing amount of evidence in literature that pain in osteoarthritis can be amplified by sensitization of the central nervous system. Moreover, preoperative characteristics of central sensitization are associated with poorer postoperative outcomes, like residual pain. Therefore preoperative treatment of central sensitization may reduce residual pain after THR/TKR. Duloxetine, a serotonin and norepinephrine reuptake inhibitor, has proven to be effective in several chronic pain syndromes in which central sensitization is believed to be involved. This trial assesses the postoperative effects on pain and function of a preoperative duloxetine treatment to a group of patients scheduled for THR/TKR and who likely suffer from a degree of central sensitization, compared to usual care.
Doel van het onderzoek
Preoperative pain treatment by means of duloxetine will improve postoperative outcome after total hip or knee arthroplasty by reducing residual pain
Onderzoeksopzet
Baseline, after two weeks, 8 weeks and 10 weeks of duloxetine treatment, 1 day before surgery, 48 hours after surgery, 6 weeks, 6 months and 12 months after surgery
Onderzoeksproduct en/of interventie
Preoperative treatment with Duloxetine for a period of 10 weeks
Publiek
Department of Orthopaedic Surgery
P.O. Box 30.001
M. Stevens
Groningen 9700 RB
The Netherlands
+31 (0)50 3613271
m.stevens@umcg.nl
Wetenschappelijk
Department of Orthopaedic Surgery
P.O. Box 30.001
M. Stevens
Groningen 9700 RB
The Netherlands
+31 (0)50 3613271
m.stevens@umcg.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Primary hip or knee osteoarthitis, age above 18 years and a neuropathic pain profile
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Surgical hip or knee procedure in previous year, hip or knee arthroscopy or injection past 3 months, unstable other medical condition, cognitive of neurological disorder or peripheral nerve injury, previous exposure to duloxetine
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL4576 |
NTR-old | NTR4744 |
Ander register | : METc nummer: 2014/087 |