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Trial registered on ANZCTR
Registration number
ACTRN12611000065998
Ethics application status
Approved
Date submitted
28/12/2010
Date registered
19/01/2011
Date last updated
19/01/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effect of zolendronic acid on the clinical resolution of acute midfoot Charcot foot
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Scientific title
The effect of zolendronic acid on the clinical resolution of acute midfoot Charcot foot
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Secondary ID [1]
253333
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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:
Charcot neuroarthropathy in patients with diabetes mellitus
258872
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Condition category
Condition code
Musculoskeletal
259009
259009
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0
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Other muscular and skeletal disorders
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Metabolic and Endocrine
259123
259123
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0
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Diabetes
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Patients with acute Charcot foot receive either 3 intravenous infusions of placebo (normal saline) or 4mg of zolendronic acid (bisphosphonate) in 4 week intervals
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Intervention code [1]
257785
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Treatment: Drugs
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Comparator / control treatment
Placebo (normal saline)
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Control group
Placebo
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Outcomes
Primary outcome [1]
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Total immobilisation time in cast
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Assessment method [1]
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Timepoint [1]
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6 months and 1 year
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Secondary outcome [1]
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Number of any surgical procedures of the affected foot during the first year of follow-up. Data is collected prospectively from patient records.
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Assessment method [1]
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Timepoint [1]
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1 year
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Eligibility
Key inclusion criteria
Patients with acute unilateral Charcot foot and type I or type II diabetes mellitus
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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
Serum creatine >400 umol/l
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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)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computerized randomization
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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 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/04/2002
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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
40
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
3113
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Finland
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State/province [1]
3113
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Pirkanmaa Hospital District
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Address [1]
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Teiskontie 35
33521 Tampere
Finland
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Country [1]
258256
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Finland
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Primary sponsor type
Hospital
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Name
Pirkanmaa Hospital District
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Address
Teiskontie 35
33521 Tampere
Finland
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Country
Finland
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Secondary sponsor category [1]
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University
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Name [1]
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Medical School, University of Tampere
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Address [1]
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Tesikontie
33521 Tampere
Finland
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Country [1]
257421
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Finland
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
260231
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Pirkanmaa Hospital Districts Ethics Commitee
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Ethics committee address [1]
260231
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Teiskontie 35 33521 Tampere Finland
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Ethics committee country [1]
260231
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Finland
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Date submitted for ethics approval [1]
260231
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10/11/2001
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Approval date [1]
260231
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11/12/2001
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Ethics approval number [1]
260231
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R01165M
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Summary
Brief summary
Diabetic Charcot foot is a rare but devastating foot complication of diabetes mellitus. The resolution of the acute form of Charcot foot needs immobilisation in a cast and total non-weight bearing for at least 12 to 16 weeks. Increased osteoclastic activity is thought to be one of the main pathological feature of the acute Charcot foot. That is why bisphosphonates are widely used in the treatment of acute Charcot process. There are some preliminary studies about the effect of bisphosphonates on the resolution of acute Charcot foot. In this study we investigated the effect of zoledronic acid on the clinical resolution of acute Charcot foot.
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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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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Toni-Karri Pakarinen
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Address
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Dept. of Orthopaedics and Traumatology
Teiskontie 35
33521 Tampere
Finland
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Country
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Finland
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Phone
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+358-3-31165009
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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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Toni-Karri Pakarinen
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Address
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Dept. of Orthopaedics and Traumatology
Teiskontie 35
33521 Tampere
Finland
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Country
6218
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Finland
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Phone
6218
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+358-3-31165009
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Fax
6218
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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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