Aarhus University
Aarhus, 8000, Denmark
NCT Number: NCT00868348
The purpose of this study is to determine wether ketorolac is effective in the treatment of postoperative pain after total knee arthroplasty
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Aarhus, 8000, Denmark
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
-
30 mg (1 ml) infiltration combined with Intraarticular bolus injection of 120 mg (4 ml) ketorolac
Other names: Toradol
1 ml infiltration 4 ml intraarticular bolus injection of placebo
Time frame: 48 hours after surgery
Consumption of intravenous (i.v.) patient-controlled analgesia (PCA) morphine during the first forty-eight hours after surgery
Time frame: within 48 hours after surgery
Time frame: 6-24 hours postoperatively
Pain intensity Visual Analogue Scale (VAS) (VAS; 0, no pain, and 100 mm, worst pain possible)
Time frame: time to fulfilment of discharge criteria
Ability to meet discharge criteria (home readiness)
Time frame: From the day of surgery until discharge
Time frame: 16 weeks after surgery
Pain intensity Visual Analogue Scale (VAS) (VAS; 0, no pain, and 100 mm, worst pain possible)
University of Aarhus
Other
Local Infiltration Analgesia for Total Knee Arthroplasty: Should Ketorolac be Added
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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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