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Trial registered on ANZCTR
Registration number
ACTRN12606000176561
Ethics application status
Approved
Date submitted
12/05/2006
Date registered
15/05/2006
Date last updated
21/01/2016
Type of registration
Prospectively registered
Titles & IDs
Public title
Effectiveness of debridement of painful plantar calluses in older people
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Scientific title
Effectiveness of scalpel debridement for the treatment of painful plantar calluses in older people: a randomised trial evaluating pain, plantar pressures and functional ability
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Secondary ID [1]
288388
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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:
Painful plantar callus (hyperkeratosis)
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Condition category
Condition code
Skin
1229
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0
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Dermatological conditions
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Scalpel debridement versus sham scalpel debridement of plantar callus
The intervention period is six weeks.
(Scalpel debridement = removal or reduction of the callus by using a scalpel or sharp blade)
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Intervention code [1]
1036
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Treatment: Other
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Intervention code [2]
293695
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Treatment: Other
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Comparator / control treatment
Sham scalpel debridement of plantar callus. The intervention period is six weeks.
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Change in pain
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Assessment method [1]
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Timepoint [1]
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Immediately post debridement and then at 1-, 3- and 6-weeks.
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Secondary outcome [1]
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Change in pain
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Assessment method [1]
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Timepoint [1]
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At 2, 4, and 5 weeks.
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Secondary outcome [2]
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Change in plantar pressures
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Assessment method [2]
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Timepoint [2]
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Immediately after debridement and then at 6-weeks post debridement.
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Secondary outcome [3]
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Change in functional tests (maximum balance range, speed to walk 6 metres, timed sit to stand test and timed alternate step test).
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Assessment method [3]
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Timepoint [3]
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Immediately after debridement and then at 6-weeks post debridement.
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Eligibility
Key inclusion criteria
Have painful plantar forefoot callus that has not been treated in the past 6 weeks•Callus must register at least 20mm on a 100mm visual analogue scale.
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Minimum age
65
Years
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Maximum age
80
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
Ability to complete the tests associated with the study (i.e. would score greater than 7 on the Short Portable Mental Status Questionnaire)•Inability to walk household distances without an aid•Has received foot orthoses in the past 2 months or will receive in the 6 week intervention period any in-shoe device that could alter the effect of the intervention•Any neurological condition that may effect sensation of the plantar surface (sole) of the feet (e.g. peripheral neuropathy associated with diabetes mellitus)•Inflammatory conditions affecting the feet (e.g. inflammatory arthritis)•History of plantar forefoot ulceration in the past 3 months•Any foreign bodies in the foot that may be causing pain•Foot amputation other than amputation of a digit or digits.
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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)
Sequentially numbered opaque (including aluminium foil) sealed envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated (using Microsoft Excel)
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Masking / blinding
Blinded (masking 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
Phase 3
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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
15/05/2006
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Actual
15/05/2006
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Date of last participant enrolment
Anticipated
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Actual
24/11/2008
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
80
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Accrual to date
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Final
80
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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La Trobe University Faculty of Health Starter Grant
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Address [1]
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La Trobe University
Vic, 3086
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Country [1]
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Australia
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Primary sponsor type
Individual
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Name
Dr Karl B Landorf
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Address
La Trobe University
Vic, 3086
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Dr Hylton B Menz
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Address [1]
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La Trobe University
Vic, 3086
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Country [1]
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Australia
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Secondary sponsor category [2]
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Individual
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Name [2]
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Adam Bird
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Address [2]
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La Trobe University
Vic, 3086
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Country [2]
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Australia
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Secondary sponsor category [3]
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Individual
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Name [3]
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Chelsey Nash
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Address [3]
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La Trobe University
Vic, 3086
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Country [3]
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Australia
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Secondary sponsor category [4]
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Individual
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Name [4]
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Anna Novak
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Address [4]
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La Trobe University
Vic, 3086
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Country [4]
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Australia
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Secondary sponsor category [5]
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Individual
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Name [5]
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Martin Spink
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Address [5]
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La Trobe University
Vic, 3086
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Country [5]
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Australia
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Secondary sponsor category [6]
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Individual
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Name [6]
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Dr Julia Potter
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Address [6]
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La Trobe University
Vic, 3086
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Country [6]
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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La Trobe University
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Ethics committee address [1]
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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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Approval date [1]
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01/05/2006
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Ethics approval number [1]
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FHEC06/25
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Summary
Brief summary
The aim of this project is to evaluate the effectiveness of reducing painful callus (hard skin) on the bottom of the feet (using scalpel debridement) versus no reduction (using a sham debridement technique). This study is double-blind: both the participants and the assessors will be blinded.
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Trial website
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Trial related presentations / publications
Journal article Landorf KB, Morrow A, Spink MJ, Nash CL, Novak A, Potter J, Menz HB: Effectiveness of scalpel debridement for painful plantar calluses in older people: a randomized trial. Trials 2013, 14:243.
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Public notes
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Contacts
Principal investigator
Name
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A/Prof Karl Landorf
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Address
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Discipline of Podiatry
School of Allied Health
La Trobe University
Vic, 3086
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Country
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Australia
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Phone
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+613 9479 5300
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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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Dr Karl B Landorf
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Address
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Discipline of Podiatry
School of Allied Health
La Trobe University
Vic, 3086
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Country
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Australia
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Phone
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(03) 9479 5300
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Fax
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(03) 9479 5784
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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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Dr Karl B Landorf
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Address
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Discipline of Podiatry
School of Allied Health
La Trobe University
Vic, 3086
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Country
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Australia
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Phone
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(03) 9479 5300
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Fax
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(03) 9479 5784
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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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