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A prospective assessment of patient outcomes following joint replacement surgery

Not Applicable
Recruiting
Conditions
Knee Arthritis
Hip Arthritis
Musculoskeletal - Osteoarthritis
Musculoskeletal - Other muscular and skeletal disorders
Surgery - Other surgery
Registration Number
ACTRN12618000317291
Lead Sponsor
A/Prof John Ireland
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
3000
Inclusion Criteria

Diagnosed with orthopaedic Hip or Knee pathology and booked for THR, TKR or UKR.
- Undergoing treatment by primary investigator/orthopaedic consultant surgeon.
- Consenting to being part of the Clinical Research Registry which is within the Sydney Bone and Joint Clinic

Exclusion Criteria

- Patient-reported outcomes: Clinically diagnosed mental/neurological illness (indicated on GP referral, or identified through secondary referral to psychiatric/neurological specialist) that precludes retrieval of patient feedback via interview, paper or electronic questionnaire (e.g., schizophrenia, dementia, Alzheimer's Disease, personality disorder).
- Revocation of consent for research use of personal data.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The incidence of patients that are deemed a failure to cure following definitive treatment, with failure to cure being considered if there is any of the following:<br>- Insufficient improvement in patient reported outcome measures (function or pain) when measured against minimally clinical important difference for the PROMs identified in secondary outcomes;<br>- Adverse findings on post-treatment medical imaging, as identified by radiologist and reported to the surgeon; <br>- Positive signs of instability, weakness or other primary pathology during clinical follow-up, measured by surgeon interpretation of ML stability and AP stability; or<br>- Failure to improve knee or hip range of motion, fixed flexion, extension lag and flexion contracture measured using a goniometer.[3months, 12months, 2years and 5years after clinical diagnosis within the specialist orthopaedic practice or following definitive treatment, depending on the specific pathology.]
Secondary Outcome Measures
NameTimeMethod
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