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Clinical Trials/NCT01323179
NCT01323179
Completed
Not Applicable

Acute Pain After Fast-track Total Knee Arthroplasty: Preoperative Opioid Versus Non-opioid

Hvidovre University Hospital4 sites in 1 country140 target enrollmentMarch 2011

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Pain
Sponsor
Hvidovre University Hospital
Enrollment
140
Locations
4
Primary Endpoint
Pain
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Observational study evaluating pain response after total knee arthroplasty (TKA) in patients taking strong, weak or no opioids preoperatively.

Registry
clinicaltrials.gov
Start Date
March 2011
End Date
February 2013
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Troels Haxholdt Lunn

MD

Hvidovre University Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients operated with elective, primary, unilateral total knee arthroplasty (TKA) (taking strong or weak opioid daily for minimum 4 weeks or opioid naive patients)

Exclusion Criteria

  • Bilateral / revision arthroplasty
  • Disease affection central or peripheral nerve function
  • Alcohol and medical abuse
  • Daily use of glucocorticoids
  • Malignancy
  • BMI \> 40
  • Dementia or other cognitive dysfunction
  • Treatment of anxiety or depression

Outcomes

Primary Outcomes

Pain

Time Frame: 24 hours

Pain during ambulation and at rest

Secondary Outcomes

  • Pain(7 days)
  • Opioid consumption(7 days)

Study Sites (4)

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