Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07464080

Advanced Brain Imaging-TKA (fMRI-TKA)

Led by Ottawa Hospital Research Institute · Updated on 2026-03-11

50

Participants Needed

1

Research Sites

143 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Knee replacement surgery is a common and effective treatment for pain and mobility loss, yet up to 1 in 5 patients remain dissatisfied after surgery due to ongoing pain or difficulty with daily activities. Currently, clinicians cannot reliably predict which patients will experience these challenges. This study uses MRI scan of the brain to investigate whether specific patterns of brain activity can predict patient satisfaction after total knee arthroplasty (TKA). By comparing brain networks before surgery and afterward, and linking these changes to patient-reported pain and function, we aim to identify brain-based markers that can help predict outcomes, to improve satisfaction after knee replacement surgery.

CONDITIONS

Official Title

Advanced Brain Imaging-TKA (fMRI-TKA)

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Male and female patients aged 18 years or older
  • Patients scheduled for their first total knee arthroplasty (primary TKA)
  • Diagnosis of osteoarthritis, inflammatory arthritis, or osteonecrosis
Not Eligible

You will not qualify if you...

  • Unable or unwilling to sign informed consent
  • Non-English or French speaking without an available translator or substitute decision maker
  • History of major neurological disorders such as traumatic brain injury, epilepsy, or multiple sclerosis
  • Cognitive impairment or dementia
  • Prior revision or bilateral total knee arthroplasty
  • Chronic opioid use

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Ottawa Hospital

Ottawa, Ontario, Canada

Actively Recruiting

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Research Team

S

Sanjula Costa

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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