Differences in knee bone density in patients with knee osteoarthritis who receive either cemented or cementless total knee arthroplasty.

Not Applicable

• Conditions: Osteoarthritis; Total Knee Arthroplasty; Arthritis; Knee Osteoarthritis; Knee Arthritis; Knee Surgery; Musculoskeletal - Osteoarthritis; Surgery - Other surgery

• Registration Number: ACTRN12621001339842
• Lead Sponsor: Monash Health

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2021-10-06
• Last Update Posted: 11 October 2021

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

1.The patient is a male or non-pregnant female.
2.The patient suffers from osteoarthritis.
3.The patient has signed the study specific, HREC-approved, Informed Consent document and is willing and able to comply with the specified pre-operative and post-operative clinical and radiographic evaluations.
4.The patient is a suitable candidate for a Cruciate Retaining cementless TKA (based on the Investigator’s clinical judgment).
5.The patient only requires uni-lateral TKA (rather than bilateral TKA).

Exclusion Criteria

1.The patient has a systemic or local condition that would limit the ability to assess the performance of the device e.g. neuromuscular or neurosensory deficiency, disorder leading to progressive bone deterioration (including rheumatoid arthritis and osteoporosis), or the patient is immunologically suppressed.
2.The patient has a cognitive impairment, an intellectual disability or a mental illness that is considered by the investigator to inhibit the patient’s capacity to consent to research and the ability to participate in it.

Study & Design

• Study Type: Interventional
• Study Design: Not specified