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Trial registered on ANZCTR
Registration number
ACTRN12605000051640
Ethics application status
Approved
Date submitted
14/07/2005
Date registered
27/07/2005
Date last updated
20/03/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
A safety study of autologous mesenchymal precursor cells (MPCs) in the management of delayed healing tibial fractures requiring secondary surgical intervention to promote fracture union.
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Scientific title
A safety study of autologous mesenchymal precursor cells in the management of delayed healing tibial fractures requiring secondary surgical intervention to promote fracture union.
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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:
Delayed or non-union tibial fracture
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Condition category
Condition code
Musculoskeletal
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Fractures
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Surgery and administration of MPCs
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Intervention code [1]
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Treatment: Other
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Comparator / control treatment
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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To assess safety of the autologous MPCs in the treatment of delayed or non-union tibial shaft fractures.
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Assessment method [1]
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Timepoint [1]
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Secondary outcome [1]
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To demonstrate fracture healing is similar or better to than the standard core intervention for delayed or non-union tibial fractures, i.e. autograft or allograft. adminstration of MPCs.
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Assessment method [1]
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Timepoint [1]
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Eligibility
Key inclusion criteria
A tibial fracture that is either delayed or a non-union that is classified according to the Association of Osteosynthesis as either 42-A, 42-B or 42-C
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Minimum age
Not stated
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Maximum age
Not stated
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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
A wound associated with the fracture that is classified according to the Gustilo Anderson Classification System as a IIIC
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Non-randomised 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)
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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
Single group
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Other design features
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Phase
Phase 1
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Type of endpoint/s
Safety
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
3/08/2006
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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
10
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
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Commercial sector/Industry
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Name [1]
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Mesoblast
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Mesoblast
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Address
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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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None
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
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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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Mr Paul Rennie
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Address
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Mesoblast
Level 39
55 Collins Street
Melbourne VIC 3000
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Country
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Australia
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Phone
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+61 3 96396037
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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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Tamara Lewis
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Address
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Mesoblast
Level 39
55 Collins Street
Melbourne VIC 3000
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Country
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Australia
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Phone
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+61 3 96396037
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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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