Preopioid Versus Nonopioid in Total Knee Arthroplasty (TKA)

NCT01323179 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 140

Last updated 2013-06-05

No results posted yet for this study

Summary

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

Conditions

  • Postoperative Pain

Sponsors & Collaborators

  • Hvidovre University Hospital

    lead OTHER

Principal Investigators

  • Troels H Lunn, MD · Dep. of Anesthesiology, Hvidovre University Hospital

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-03-31
Primary Completion
2013-02-28
Completion
2013-02-28

Countries

  • Denmark

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01323179 on ClinicalTrials.gov