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Preopioid Versus Nonopioid in Total Knee Arthroplasty (TKA)

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01323179
Enrollment
140
Registered
2011-03-25
Start date
2011-03-31
Completion date
2013-02-28
Last updated
2013-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

Postoperative pain, Postoperative opioid requirements

Brief summary

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

Interventions

None listed

Sponsors

Hvidovre University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Pain24 hoursPain during ambulation and at rest

Secondary

MeasureTime frameDescription
Pain7 daysPain during ambulation and at rest
Opioid consumption7 days

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026