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Trial registered on ANZCTR
Registration number
ACTRN12615000845538
Ethics application status
Approved
Date submitted
21/07/2015
Date registered
14/08/2015
Date last updated
4/05/2018
Type of registration
Prospectively registered
Titles & IDs
Public title
Randomised control trial of less Invasive Piriformis sparing Hip Approach: 10 year Follow-up
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Scientific title
Randomised control trial of less Invasive Piriformis sparing Hip Approach: 10 year Follow-up
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Secondary ID [1]
287088
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nil
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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:
Total Hip Arthroplasty
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Condition category
Condition code
Surgery
295875
295875
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0
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Surgical techniques
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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
10 year follow-up of patient that underwent piriformis sparing approach compared to standard posterior approach as described in A comparison of a less invasive piriformis-sparing approach versus the standard posterior approach to the hip, A randomised Control Trial. Khan, Maor, Hofmann and Haebich, The Journal of Bone & Joint Surgery. 94 B (1) jan 2012.
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Intervention code [1]
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Not applicable
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Comparator / control treatment
standard posterior approach for total hip arthroplasty
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Control group
Active
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Outcomes
Primary outcome [1]
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Functional disability assessed using the Oxford Hip Score
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Assessment method [1]
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Timepoint [1]
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10 year
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Primary outcome [2]
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Short Form 12
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Assessment method [2]
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Timepoint [2]
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10 year
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Primary outcome [3]
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ability and endurance to mobilise is assessed 6 minute walk test
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Assessment method [3]
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Timepoint [3]
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10 year
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Secondary outcome [1]
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Subjective personal health concerns and complications will be assessed using a general health questionnaire
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Assessment method [1]
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Timepoint [1]
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10 year
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Eligibility
Key inclusion criteria
Patients previously recruited for A comparison of a less invasive piriformis-sparing approach versus the standard posterior approach to the hip, A randomised Control Trial. Khan, Maor, Hofmann and Haebich, The Journal of Bone & Joint Surgery. 94 B (1) jan 2012.
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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
revision surgery on the included hip
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
Population is based on previous trial: A comparison of a less invasive piriformis-sparing approach versus the standard posterior approach to the hip, A randomised Control Trial. Khan, Maor, Hofmann and Haebich, The Journal of Bone & Joint Surgery. 94 B (1) jan 2012.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/09/2015
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Actual
1/12/2015
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Date of last participant enrolment
Anticipated
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Actual
1/06/2017
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Date of last data collection
Anticipated
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Actual
1/06/2017
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Sample size
Target
80
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Accrual to date
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Final
191
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Sir Charles Gairdner Hospital - Nedlands
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Funding & Sponsors
Funding source category [1]
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Self funded/Unfunded
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Name [1]
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Address [1]
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Country [1]
291690
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Primary sponsor type
Hospital
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Name
Sir Charles Gairdner Hospital
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Address
Hospital Ave, Nedlands WA 6009
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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]
290365
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Country [1]
290365
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Sir Charles Gairdner Hospital
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Ethics committee address [1]
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Hospital Ave, Nedlands WA 6009
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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26/07/2015
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Approval date [1]
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20/11/2015
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Ethics approval number [1]
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HREC No: 2015-125
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Summary
Brief summary
To assess the long term quality of the tendon, it’s isometric strength and the clinical outcomes of a piriformis sparing approach to total hip arthroplasty as compared to a standard posterior approach. A randomised, controlled cohort of 100 patients previously followed to the 5 year period will be assessed at 10 year follow-up with clinical scores.
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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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Dr Craig Brownlie
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Address
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Sir Charles Gairdner Hospital,
Hospital Ave, Nedlands
WA 6009
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Country
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Australia
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Phone
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+61417793837
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Sam Haebich
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Address
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The Joint Studio
Suite 1, 85 Monash Avenue
Hollywood Medical Centre
Nedlands, Western Australia 6009
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Country
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Australia
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Phone
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+61417793837
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Craig Brownlie
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Address
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Sir Charles Gairdner Hospital,
Hospital Ave, Nedlands
WA 6009
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Country
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Australia
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Phone
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+61417793837
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
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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