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Clinical Trials/NCT01863342
NCT01863342
Unknown
Not Applicable

Influence of Central Sensitization on Efficacy of Patient-controlled Epidural Analgesia in Osteoarthritis Patients Undergoing Total Knee Replacement

Yonsei University1 site in 1 country98 target enrollmentMay 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Knee Osteoarthritis
Sponsor
Yonsei University
Enrollment
98
Locations
1
Primary Endpoint
Peak pain score
Last Updated
12 years ago

Overview

Brief Summary

Nociceptor inputs can trigger a prolonged but reversible increase in the excitability and synaptic efficacy of neurons in central nociceptive pathways, the phenomenon of central sensitization. The degenerative joint disease, osteoarthritis, with characteristic destruction of cartilage and alteration in bone is a very common cause of chronic pain. The degree of pain does not always correlate with the extent of joint damage or presence of active inflammation raising the possibility that there may be a central component to the pain. The central sensitization inventory (CSI) is a new self-report screening instrument to measure the degree of central sensitization, and to help identify patients with central sensitivity syndromes. The aim of this investigation is to evaluate the influence of preoperative central sensitization, which represented by CSI score, on postoperative pain score in osteoarthritis patients undergoing total knee replacement who receiving patient-controlled epidural analgesia.

Registry
clinicaltrials.gov
Start Date
May 2013
End Date
May 2014
Last Updated
12 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Aged 20 to 80 years osteoarthritis patients undergoing total knee replacement under spinal anesthesia, and who receiving postoperative epidural PCA

Exclusion Criteria

  • coagulopathy
  • neurologic deficit
  • preoperative opioids medication
  • recent analgesics change

Outcomes

Primary Outcomes

Peak pain score

Time Frame: at the point of Epidural PCA to postoperative 1-48 h

Numeric rating scale (0 to 10 points) at each assessment interval

Study Sites (1)

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