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Clinical Trials/NCT01179204
NCT01179204
Completed
Not Applicable

Is Preoperative Pain Response Upon Tonic Heat Stimulation Predictive for Pain After Total Knee Arthroplasty?

Hvidovre University Hospital1 site in 1 country100 target enrollmentAugust 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain, Postoperative
Sponsor
Hvidovre University Hospital
Enrollment
100
Locations
1
Primary Endpoint
Cumulated pain (from 0-24 hours after surgery)
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

In this consecutive, prospective cohort study trial the investigators evaluate if preoperative pain response upon heat stimulation is predictive for acute and subacute postoperative pain after total knee arthroplasty.

Detailed Description

The preoperative heat stimulation consists of short and long tonic heat stimulation. Pain response is evaluated with an electronic visual analog scale. Furthermore the investigators evaluate other factors possibly predictable for acute and subacute postoperative pain after total knee arthroplasty - demographic factors, preoperative pain related factors, psychosocial factors (Hospital Anxiety and Depression Scale and Pain Catastrophizing Scale).

Registry
clinicaltrials.gov
Start Date
August 2010
End Date
September 2011
Last Updated
13 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

  • Ethnic danes, above 18 years and able to give informed consent scheduled for primary, unilateral total knee arthroplasty.

Exclusion Criteria

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

Outcomes

Primary Outcomes

Cumulated pain (from 0-24 hours after surgery)

Time Frame: 24 hours

Pain during walk 5 m (VAS)

Secondary Outcomes

  • Cumulated pain (from day 1 to day 7 after surgery)(7 days)
  • Pain at day 14 after surgery(14 days)
  • Pain at day 30 after surgery(30 days)

Study Sites (1)

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