Gentofte Hospital
Hellerup, 2900, Denmark
NCT Number: NCT02254499
Despite improvements in treatment, a significant part of patients have severe pain following knee arthroplasty. Preoperative identification of high-risk patients would allow for an intensive individualized analgesic treatment pre- and postoperatively and thus potentially in reduced pain acute and chronically.
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Notify Me50 year–80 year
All sexes
Observational
Hellerup, 2900, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 24 hours postoperatively
Pain intensity on a NRS from 0 to 10 upon ambulation 24 hours following surgery
Time frame: 48 hours postoperatively
Pain intensity on a NRS (numeric rank scale) from 0 to 10 upon ambulation 48 hours following surgery
Time frame: From day 1 to day 14 following surgery
Daily diary reported pain intensity on a NRS (numeric rank scale) from 0 to 10 in average and when worse the first two weeks following knee arthroplasty.
Rigshospitalet, Denmark
Other
Prospective Descriptive Study of Nociceptive and Psychological Prediction of Pain After Total Knee Arthroplasty (TKA)
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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