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Prediction of Pain in Total Hip Arthroplasty

H

Hvidovre University Hospital

Status

Completed

Conditions

Pain, Postoperative

Treatments

Device: heat pain test (Modular Sensory Analyzer, Somedic AB, Horby, Sweden).

Study type

Observational

Funder types

Other

Identifiers

NCT01324375
H-2-2010-052, part 2

Details and patient eligibility

About

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

Full 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 hip arthroplasty - demographic factors, preoperative pain related factors, psychosocial factors (Hospital Anxiety and Depression Scale and Pain Catastrophizing Scale).

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Trial design

60 participants in 1 patient group

THA (total hip arthroplasty)
Description:
Patients undergoing THA, preoperatively heat tested
Treatment:
Device: heat pain test (Modular Sensory Analyzer, Somedic AB, Horby, Sweden).

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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