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Prediction of Outcomes Following Total Knee Replacement

Prediction of Outcomes Following Total Knee Replacement

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01370421
Acronym
POKR
Enrollment
248
Registered
2011-06-10
Start date
2011-04-30
Completion date
2019-03-31
Last updated
2022-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis

Brief summary

This is an observational study (not a treatment study) of pain and physical functioning after total knee replacement. The study includes 5 visits, 1 before surgery and 4 after surgery. You may be eligible if you are 50 or older,will soon be undergoing knee replacement surgery, do not have a serious heart condition or certain other medical conditions, and are not taking certain types of medications. The study includes evaluation of peoples' pain, physical functioning, medication use, and physiological responses to sensory stimuli such as heat and cold.

Detailed description

This is an observational study (not a treatment study) of pain and physical functioning after total knee replacement. The study includes 5 visits, 1 before surgery and 4 after surgery. The last visit will be about 1 year after surgery. You may be eligible if you are 50 or older, will soon be undergoing knee replacement surgery, do not have a serious heart condition or certain other medical conditions, and are not taking certain types of medications. The study includes evaluation of peoples' pain, physical functioning, medication use, and physiological responses to sensory stimuli such as heat and cold.

Interventions

None listed

Sponsors

Brigham and Women's Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age 50 or older * Meet the American College of Rheumatology criteria for knee osteoarthritis * Scheduled to undergo total knee arthroplasty * Facility with the English language that is adequate to complete study procedures

Exclusion criteria

* Cognitive impairment preventing completion of study assessment procedures * Myocardial infarction within the past 12 months * Severe raynaud's or severe neuropathy * Active vasculitis or severe peripheral vascular disease * Current infection * Use of oral steroids * Recent history of substance abuse or dependence * Confirmed diagnosis of periodic limb movement disorder or restless legs syndrome * Systemic inflammatory or autoimmune disorders such as rheumatoid arthritis, lupus, etc. * Known anemia

Design outcomes

Primary

MeasureTime frameDescription
Brief Pain Inventory (BPI)6 monthsA widely-used measure of pain severity and pain interference. Pain severity and pain interference scores range from 0-10 (0= no pain / no pain interference and 10= severe pain / pain interference).
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)6 monthsA widely-used, OA-specific measure of pain, function, and stiffness. WOMAC Pain scores range from 0-50, with 0= no pain and 50= severe pain.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026