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Trial registered on ANZCTR
Registration number
ACTRN12617000550303
Ethics application status
Approved
Date submitted
30/03/2016
Date registered
19/04/2017
Date last updated
7/10/2021
Date data sharing statement initially provided
7/10/2021
Date results provided
7/10/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
A prospective, observational, cohort study of the MASTER-SL Femoral stem in patients with degenerative disease of the hip
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Scientific title
In patients with Osteoarthritis of the hip undergoing a Total Hip Replacement, how does the MASTER-SL femoral stem perform under standard conditions with regards to clinical outcomes.
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Secondary ID [1]
283934
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Osteoarthritis
290953
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Condition category
Condition code
Musculoskeletal
291299
291299
0
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
50 patients to undergo Total Hip Replacement, the prosthesis used for the trial is MASTER-SL femoral stem. Patients will be followed up for functional and radiological assessments and side effects for a minimum of two years post surgery.
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Intervention code [1]
288630
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Diagnosis / Prognosis
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Comparator / control treatment
Nil
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
291297
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Clinical Outcome Scores: harris Hip Score,
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Assessment method [1]
291297
0
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Timepoint [1]
291297
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Pre-Operative, 6 weeks post op, 6 months post-op, 1 year post op, 2 year Post op
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Primary outcome [2]
298090
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Outcome score: Oxford Hip
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Assessment method [2]
298090
0
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Timepoint [2]
298090
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Pre-Operative, 6 weeks post op, 6 months post-op, 1 year post op, 2 year Post op
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Primary outcome [3]
298091
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Outcome score: Non arthritic hip score
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Assessment method [3]
298091
0
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Timepoint [3]
298091
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Pre-Operative, 6 weeks post op, 6 months post-op, 1 year post op, 2 year Post op
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Secondary outcome [1]
306445
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Outcome Score: EQ5D 5L
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Assessment method [1]
306445
0
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Timepoint [1]
306445
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Pre-Operative, 6 weeks post op, 6 months post-op, 1 year post op, 2 year Post op
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Secondary outcome [2]
323150
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Revision surgery during the observation follow up period due to prosthesis failure
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Assessment method [2]
323150
0
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Timepoint [2]
323150
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2 year follow up
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Eligibility
Key inclusion criteria
Male and female >18 years;
radiologically confirmed diagnosis of primary osteoarthritis (OS) of the hip and suitable for primary total hip replacement;
Life expectancy of > 10 years
Receiving a MASTER-SL femoral stem
Voluntary written informed consent obtained
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Minimum age
18
Years
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Maximum age
No limit
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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
Prospect for recovery to independent mobility compromised by known coexistent, medical problems;
Requiring revision hip replacement;
Loss of abductor musculature, poor bone stock, or poor skin coverage around the hip join;
Previous organ transplant;
Previous hip replacement (resurfacing or THR) on the contra-lateral side within the last 6 months;
Previous hip replacement (resurfacing or THR) on the contralateral side and whose outcome is achieving an Oxford Hip score <18 points;
Body mass index > 40 kg/m2
Active or suspected infection;
Known sensitivity to device materials;
Pregnant woman
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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
Prospective
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Statistical methods / analysis
The National Institute for Health and Clinical Excellence (NICE) "benchmark" for hip prostheses is a revision rate of 10% or less over a 10 year period. Data in the current study will be used to determine revision rates for this study population and will be determined using Kaplan-Meier methods. The Orthopaedic Data Evaluation Panel (ODEP) which advises the NHS Supply Chain, require 10 years of followup in at least 500 patients across 3 or more center to be able to classify the evidence for clinical effectiveness of a prosthesis as "strong". Data from this study will support global data to evaluate the ODEP rating for this device.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
28/10/2014
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Date of last participant enrolment
Anticipated
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Actual
30/10/2015
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Date of last data collection
Anticipated
30/10/2017
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Actual
30/10/2017
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Sample size
Target
50
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Accrual to date
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Final
50
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment postcode(s) [1]
7708
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4812 - Pimlico
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Funding & Sponsors
Funding source category [1]
288578
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Commercial sector/Industry
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Name [1]
288578
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Lima Orthopaedics Australia Pty Ltd
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Address [1]
288578
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Unit 1, 40 Ricketts Rd
Mt Waverley 3149
Victoria-Australia
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Country [1]
288578
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Australia
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Primary sponsor type
Other
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Name
The Orthopaedic Institute of Queensland (ORIQL)
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Address
Suite 102 Level 2 Mater Medical Centre
21-37 Fulham Road
Pimlico QLD 4812
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Country
Australia
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Secondary sponsor category [1]
287288
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None
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Name [1]
287288
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Nil
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Address [1]
287288
0
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Country [1]
287288
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
290441
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Mater Hospital Townsville Ethics Committee
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Ethics committee address [1]
290441
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Mater Hospital Townsville 21-37 Fulham Rd Pimlico QLD 4810
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Ethics committee country [1]
290441
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Australia
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Date submitted for ethics approval [1]
290441
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11/02/2014
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Approval date [1]
290441
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11/02/2014
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Ethics approval number [1]
290441
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Summary
Brief summary
Factors for operative treatment include severity of diseases that affect the hip, symptoms, clinical finding on physical examination and radiological assessment of the hip. When referring to total hip replacement (THR) surgery, both the acetabular socket and the head of the femur are replaced with a suitable prosthetic device consisting of a cup fitted into the acetabulum (socket) and a new head (ball) with stem fitted into the upper shaft of the femur. Two major factors influence the outcome of THR (outside the surgery process itself) and these are the fixation of the components to the bone and wear of the implanted surfaces. (between the ball and socket). THR is an extremely successful operation due to continuous improvements in surgical techniques, bio-materials and implant design. It is necessary however, to safely evaluate new advances in the design of hip replacement components so that improvements are sought to continually enhance patient outcomes. The design and materials used in the MASTER-SL femoral implant are very similar to other prosthesis already used by surgeons. The aim of this trial is to assess the clinical performance of the MASTER-SL femoral stem over a two year period under standard condition of use in THR.
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Trial website
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Trial related presentations / publications
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Public notes
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Attachments [1]
173
173
0
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/AnzctrAttachments/365639-Hrec approval 16 may 2014.pdf
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Attachments [2]
174
174
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/AnzctrAttachments/365639-Section 2 signed ARTG CTN.pdf
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Attachments [3]
175
175
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/AnzctrAttachments/365639-Section 4 signed ARTG CTN.pdf
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Attachments [4]
176
176
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/AnzctrAttachments/365639-CTN - CID52569 - MHS20140211-3 - 2014 0417 - Mater Health Services Nth Q .pdf
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Contacts
Principal investigator
Name
45614
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Dr Kaushik Hazratwala
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Address
45614
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The Orthopaedic Research Institute of Queensland Suite 102 Level 2 Mater Medical Centre 21-29 Fulham Rd Pimlico 4812 Qld
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Country
45614
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Australia
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Phone
45614
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+61 7 47550564
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Fax
45614
0
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Email
45614
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[email protected]
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Contact person for public queries
Name
45615
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Andrea Grant
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Address
45615
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The Orthopaedic Research Institute of Queensland
7 Turner Street, Pimlico, Townsville, QLD Australia. 4812
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Country
45615
0
Australia
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Phone
45615
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+61 7 413685331
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Fax
45615
0
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Email
45615
0
[email protected]
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Contact person for scientific queries
Name
45616
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Andrea Grant
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Address
45616
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The Orthopaedic Research Institute of Queensland
7 Turner Street, Pimlico, Townsville, QLD Australia. 4812
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Country
45616
0
Australia
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Phone
45616
0
+61 7 47550564
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Fax
45616
0
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Email
45616
0
[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
Source
Title
Year of Publication
DOI
Embase
Short-term results of a new self-locking cementless femoral stem: a prospective cohort study of the Lima MasterSL.
2021
https://dx.doi.org/10.1007/s12306-020-00651-1
N.B. These documents automatically identified may not have been verified by the study sponsor.
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