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Trial registered on ANZCTR
Registration number
ACTRN12612000028808
Ethics application status
Approved
Date submitted
22/07/2008
Date registered
9/01/2012
Date last updated
23/10/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
Weight Bearing in the Treatment of Acute Achilles Tendon Ruptures: A Randomised Controlled Trial
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Scientific title
Weight bearing versus non-weight bearing casts in the treatment of acute achilles tendon ruptures: effects on re-rupture rate and functional outcomes
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Secondary ID [1]
279675
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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:
Achilles tendon ruptures
3439
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Condition category
Condition code
Musculoskeletal
3593
3593
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Weightbearing group - Gravity equinus cast applied over foot/lower leg for a total of 8 weeks. cast applied straight after allocation. These patients received a bohler iron attachement to their cast from day 1.
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Intervention code [1]
3172
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Treatment: Other
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Intervention code [2]
283921
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Treatment: Devices
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Comparator / control treatment
Non-weightbearing group - Gravity equinus cast applied over foot/lower leg for a total of 8 weeks. cast applied straight after allocation. These patients did not receive a bohler iron at anytime.
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Control group
Active
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Outcomes
Primary outcome [1]
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Return to work via telephone follow-up call
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Assessment method [1]
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Timepoint [1]
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3 months after the cast has been applied.
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Secondary outcome [1]
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Rerupture Rate via hospital database search
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Assessment method [1]
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Timepoint [1]
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one year after interventional commencement, ie time of casting
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Eligibility
Key inclusion criteria
Unilateral acute rupture
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Minimum age
15
Years
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Maximum age
60
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
Previous injury
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
All patients presenting to Northshore and Middlemore hospitals with in the study period with an acute achilles tendon rupture were offered enrolment, once enrolled, the patients were allocated to either group using a numbered, sealed and sequential envelope generated by a thrid party with no affiliations centrally
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
computer generated, no stratification was done or was felt to be neccessary
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/01/2008
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Actual
4/09/2007
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Date of last participant enrolment
Anticipated
1/01/2009
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Actual
24/04/2010
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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New Zealand
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State/province [1]
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Auckland, New Zealand
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Funding & Sponsors
Funding source category [1]
3621
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Charities/Societies/Foundations
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Name [1]
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Wishbone Trust
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Address [1]
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New Zealand Orthopaedic Association
Level 12
Greenock House
39 The Terrace
Wellington 6011
New Zealand
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Country [1]
3621
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New Zealand
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Primary sponsor type
Hospital
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Name
Middlemore Hospiital
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Address
Middlemore Hospital
100 Hospital Road
Otahuhu 2025
Auckland
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Country
New Zealand
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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]
3256
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Country [1]
3256
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Northern X ethics committee
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Ethics committee address [1]
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3rd floor, Unisys building 650 Great South Rd Penrose Auckland 1061
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Ethics committee country [1]
5673
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New Zealand
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Date submitted for ethics approval [1]
5673
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Approval date [1]
5673
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04/06/2007
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Ethics approval number [1]
5673
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NTX0705047
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Summary
Brief summary
Acute achilles tendon ruptures are increasing in incidence, however there remains a lack of consensus on the optimum treatment for acute ruptures. Non surgical treatment is favoured in many parts of the world and it is unclear what is the best post operative protocol. we believe that early weight bearing may assist in the healing of the tendon resulting in better functional outcomes and faster return to work. This study aims investigate whether early weightbearing with a bohler iron is beneficial for conservatively treated patients with acute achilles tendon ruptures
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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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Mr Simon Young
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Address
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North Shore Hospital, Shakespeare Road, Takapuna, Auckland, New Zealand
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Country
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New Zealand
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Phone
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640273654986
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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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Simon Young
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Address
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Northshore hospital, 124 Shakespeare Road, Westlake 0622, Auckland
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Country
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New Zealand
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Phone
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+64 21616183
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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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Matt Tomlinson
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Address
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Middlemore hospital, 100 Hospital Road, Papatoetoe 2025, Auckland
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Country
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New Zealand
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Phone
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+64 9 2760000
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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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