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A prospective assessment of patient outcomes following joint replacement surgery

A prospective assessment of patient outcomes following joint replacement surgery performed by a single surgeon in private practice

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12618000317291
Acronym
PAPOJRS
Enrollment
2358
Registered
2018-03-02
Start date
2010-03-10
Completion date
2028-12-31
Last updated
2023-01-09

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

Conditions

None listed

Brief summary

This is a prospective, observational cohort study assessing patient outcomes after joint replacement surgery. The purpose of this study is to assess clinical outcomes within the Investigator’s practice. The primary objective of this protocol is the implementation of an ongoing registry to collate and store patient outcomes collected routinely as part of the standard clinical pathway for hip and knee arthroplasty at the Investigator’s practice. Outcomes will include objective joint function, pain, satisfaction, quality of life, radiology and revision surgery. The secondary objective is to integrate the clinical outcomes with analyses provided by the Australian National Joint Replacement Registry. Recruitment will include all patients electing to undergo hip or knee arthroplasty surgery within the investigator's practice. Patients will undergo standard of care preoperative work-up, including the collection of demographic, medical history, radiology, pathology, and functional analysis. Patients will be required to complete the; EQ-5D 5L, and specific joint function outcomes will include Harris Hip Score (HHS), Oxford Hip Score (OHS), Oxford Knee Score (OKS), International Knee Society score (IKSS). Patient evaluation will be completed at the following time points: preoperatively and postoperatively at 2 to 6 weeks, 3 months, 12 months, 24 months and 5 years. The clinical outcomes of individual patients will be monitored up to 5 years postoperatively.

Interventions

Patients presenting with pathologies of the knee or hip and referred to specialist orthopaedic review and undergoing a Total Knee Replacement, Unicompartmental Knee Replacement or Total Hip Replacement. 1. Patients diagnosed with knee arthritis of any aetiology: Treated total knee arthroplasty or unicomparmental knee arthroplasty. Followed for a duration of 5 years. 2. Patients diagnosed with hip arthritis of any aetiology: Treated total hip arthroplasty. Followed for a duration of 5 years.

Sponsors

A/Prof John Ireland
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

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.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 25, 2026