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Trial registered on ANZCTR
Registration number
ACTRN12621000555853p
Ethics application status
Submitted, not yet approved
Date submitted
9/03/2021
Date registered
12/05/2021
Date last updated
12/05/2021
Date data sharing statement initially provided
12/05/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
Radiological Evaluation of the Performance of the Cementless Quadra-P Stem used for Total Hip Arthroplasty.
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Scientific title
Clinical and Radiographic Performance of the Cementless Quadra-P Stem: A Retrospective and Prospective Observational Cohort Study of Adults Requiring Total Hip Arthroplasty
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Secondary ID [1]
303608
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None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
This study is a sub-study related and being run in conjunction to registration record ACTRN12620000441910.
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Health condition
Health condition(s) or problem(s) studied:
Hip Osteoarthritis
320978
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Condition category
Condition code
Musculoskeletal
318787
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0
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Osteoarthritis
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Total Hip Arthroplasty (THA) is a procedure commonly performed in patients who have end-stage hip osteoarthritis. Patients who are planned to undergo THA surgery and fit the eligibility criteria will be considered for enrollment in this study. Each participant will receive the new hydroxyapatite coated Quadra-P femoral stem together with either the Mpact or Versafit cementless acetabular component articular systems, as part of routine treatment for total hip replacement procedures. These devices will be implanted by qualified and experienced orthopaedic surgeons as per routine practice.
The newly designed Quadra-P stem device was recently introduced into the Australian market (TGA approval granted 27th February 2019), however, its short and long-term clinical and radiological performance is yet to be evaluated. The AOANJRR is currently undertaking a registry-nested clinical trial (Medacta Quadra-P Femoral Stem, ACTRN12620000441910.) investigating the survivorship and patient reported outcomes (PROMs) following implantation of the Quadra-P stem in patients undergoing total hip replacement. However, it is currently unknown whether the new Quadra-P device reduces or has the same level of risk of loosening, fractures and implant displacement, compared to other commercially available stems. The purpose of this current investigation will be to determine the radiological performance of the Quadra-P stem in providing implant stability to ensure it performs as well as or better than other commercially available stems. Patients will be retrospectively recruited and all those who have already consented to be a part of the Quadra-P stem registry-nested PROMs study (ACTRN12620000441910) will be invited to participate in the radiological study.
Several radiological measurements will be taken in order to evaluate the performance and stability of the Quadra-P stem. Patients will be required to have an x-ray of their replaced hip (of approximately 30 minutes duration) at 4 different time points (6-weeks, 1-year, 2-years and 5-years post-op) The specific measurements that will be collected include presence of radiolucencies (femur and acetabulum), leg length discrepancy, global offset reconstructions, stem alignment, stem subsidence and presence of femoral fracture. All patients whp
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Intervention code [1]
319933
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Not applicable
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Presence of Radiolucencies as assessed by x-ray
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Assessment method [1]
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Timepoint [1]
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2-years post-surgery
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Secondary outcome [1]
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Presence of Leg length discrepancy as assessed by x-ray
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Assessment method [1]
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Timepoint [1]
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6-weeks, 1-year, 2-years and 5-years post-surgery
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Secondary outcome [2]
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Presence of Global Offset Reconstruction as assessed by x-ray
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Assessment method [2]
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Timepoint [2]
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6-weeks, 1-year, 2-years and 5-years post-surgery
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Secondary outcome [3]
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Degree of stem alignment as assessed by x-ray
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Assessment method [3]
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Timepoint [3]
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6-weeks, 1-year, 2-years and 5-years post-surgery
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Secondary outcome [4]
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Degree of stem subsidence as assessed by x-ray
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Assessment method [4]
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Timepoint [4]
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6-weeks, 1-year, 2-years and 5-years post-surgery
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Secondary outcome [5]
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Presence of Radiolucencies as assessed by x-ray
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Assessment method [5]
392665
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Timepoint [5]
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6-weeks, 1 year and 5 years post-surgery
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Secondary outcome [6]
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Presence of femoral fracture as assessed by x-ray
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Assessment method [6]
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Timepoint [6]
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6-weeks, 1-year, 2-years and 5-years post-surgery
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Eligibility
Key inclusion criteria
• Patients agreed to participate in the Quadra-P Femoral Stem Study (ACTRN12620000441910. University of South Australia HREC project ID: 202658)
• Adults aged between 18 and 75 years at the time of registration.
• Patients able to give informed consent.
• Patients who are informed of the conditions of the study and are willing to participate for the length of the prescribed follow-up period.
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Minimum age
18
Years
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Maximum age
75
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
• Patients with Rheumatoid arthritis.
• Patients with a history of active infection.
• Any case not described in the inclusion criteria.
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Both
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Statistical methods / analysis
Stem radiological performance will be assessed via the specified parameters at 1-year, 2-years at 5-years post-surgery and compared to baseline x-ray obtained at 6-weeks. Any presence of radiolucencies, leg length discrepancies, changes in stem alignment, femoral fracture, global offset reconstruction or stem subsidence will be documented.
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
21/06/2021
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
75
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,VIC
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Medacta Australia Pty Ltd
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Address [1]
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Unit A1, 16 Mars Road,
Lane Cove NSW 2066
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Country [1]
308028
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Medacta Australia Pty Ltd
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Address
Unit A1, 16 Mars Road,
Lane Cove NSW 2066
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
308799
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Country [1]
308799
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Ethics approval
Ethics application status
Submitted, not yet approved
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Ethics committee name [1]
308018
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St Vincents Hospital Melbourne HREC
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Ethics committee address [1]
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Research Governance Unit Level 5, Building E 27 Fitzroy Parade Fitzroy VIC 3065
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Ethics committee country [1]
308018
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Australia
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Date submitted for ethics approval [1]
308018
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02/03/2021
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Approval date [1]
308018
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Ethics approval number [1]
308018
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Summary
Brief summary
Total Hip Arthroplasty (THA) is a procedure commonly performed in patients who have end-stage hip osteoarthritis. The primary goal of THA is to provide pain relief, reduce disability, improve quality of life and functional status. Despite high implant success rates, up to 15% of patients remain dis-satisfied after surgery. This has been postulated to be due to several factors, including implant loosening, stem fractures and reduced functional movement, which lead to poorer patient outcomes. Recently, a new range of hip replacement devices have been engineered to address some of the shortcomings of existing stems. In particular, the Quadra-P stem has specifically been designed as a straight, triple tapered stem with a rectangular cross-section and manufactured with Ti-6Al-7Nb alloy material to increase osseointegration and reduce wear. The newly designed Quadra-P stem device was recently introduced into the Australian market, however, its radiological performance is yet to be evaluated. It is currently unknown whether the new Quadra-P device reduces or has the same level of risk of loosening, fractures and implant displacement, compared to other commercially available stems. The purpose of this current investigation will be to evaluate the radiological performance of the Quadra-P stem in providing implant stability in patients undergoing THA.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Phong Tran
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Address
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Associate Professor Phong Tran Private Consulting Rooms
Specialist Orthopaedic Surgery Clinic
Ground Floor, St Francis Building
166 Gipps Street
East Melbourne, Victoria, 3002
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Country
109250
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Australia
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Phone
109250
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+61399286161
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Fax
109250
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Email
109250
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[email protected]
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Contact person for public queries
Name
109251
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Phong Tran
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Address
109251
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Associate Professor Phong Tran Private Consulting Rooms
Specialist Orthopaedic Surgery Clinic
Ground Floor, St Francis Building
166 Gipps Street
East Melbourne, Victoria, 3002
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Country
109251
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Australia
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Phone
109251
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+61399286161
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Fax
109251
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Email
109251
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[email protected]
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Contact person for scientific queries
Name
109252
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Phong Tran
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Address
109252
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Associate Professor Phong Tran Private Consulting Rooms
Specialist Orthopaedic Surgery Clinic
Ground Floor, St Francis Building
166 Gipps Street
East Melbourne, Victoria, 3002
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Country
109252
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Australia
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Phone
109252
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+61399286161
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Fax
109252
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Email
109252
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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