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Trial registered on ANZCTR
Registration number
ACTRN12609000311257
Ethics application status
Approved
Date submitted
12/02/2009
Date registered
19/05/2009
Date last updated
19/05/2009
Type of registration
Retrospectively registered
Titles & IDs
Public title
Breast reconstruction for breast asymmetry by tissue engineering
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Scientific title
Breast reconstruction for breast asymmetry by tissue engineering
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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:
breast asymmetry
4326
0
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Condition category
Condition code
Surgery
4561
4561
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0
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Surgical techniques
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Breast reconstruction in an implanted acrylic spacer using the body's own ability to grow new tissue to fill the empty space provided by acrylic spacer over a perioid of 3 to 6 months.
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Intervention code [1]
4056
0
Treatment: Surgery
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Comparator / control treatment
n/a
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Improved breast symmetry. New tissue growth will be measured using Magnetic Resonance Imaging (MRI)
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Assessment method [1]
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Timepoint [1]
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Outcome will be measured 3 months post-operatively, and after that monthly from 3-6 months post-surgery until the spacer is filled with new tissue.
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Secondary outcome [1]
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Improved breast symmetry and cosmetic result, monitored clinically by plastic surgeons
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Assessment method [1]
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Timepoint [1]
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1 year post-surgery
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Eligibility
Key inclusion criteria
Breast asymmetry, unlikely suitable for other reconstructive flap methods.
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Minimum age
18
Years
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Maximum age
70
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Previous chest wall irradiation
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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
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Who is / are masked / blinded?
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Intervention assignment
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Date of first participant enrolment
Anticipated
1/03/2009
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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
5
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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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Charities/Societies/Foundations
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Name [1]
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Microsurgical Research Foundation
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Address [1]
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Bernard O'Brien Institute of Microsurgery (BOBIM)
42 Fitzroy Street
Fitzroy, VIC 3065
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Country [1]
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Australia
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Primary sponsor type
Charities/Societies/Foundations
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Name
Microsurgical Research Foundation
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Address
Bernard O'Brien Institute of Microsurgery (BOBIM)
42 Fitzroy Street
Fitzroy, VIC 3065
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Country
Australia
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Secondary sponsor category [1]
4061
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None
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Name [1]
4061
0
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Address [1]
4061
0
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Country [1]
4061
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Human Research Ethics Committee-D St Vincent's Health Melbourne
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Ethics committee address [1]
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PO Box 2900 Fitzroy Victoria 3065
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
6558
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Approval date [1]
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11/02/2009
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Ethics approval number [1]
6558
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156/08
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Summary
Brief summary
Study hypothesis: The human body has a natural capacity to regenerate and to grow new tissue to fill an empty space. This study applies a new method of breast reconstruction using the patient’s own regenerative capacity. This method provides an alternative to current breast reconstruction techniques and also an opportunity for patients who have no other option for reconstruction. In the operation an acrylic spacer, shaped according to the breast defect, will be placed under the skin of the chest wall to allow a piece of fat with a blood supply to grow over time (3-6 months) to fill the space created by the acrylic spacer. The small piece of fat with a blood supply will be sourced from well-known existing donor sites for breast reconstruction (chest or abdomen). Because the amount of tissue is small the expected donor site scars will be smaller compared with the usual reconstruction methods.
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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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Prof Wayne Morrison
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Address
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BOBIM
42 Fitzroy Street
Fitzroy, VIC 3065
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Country
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Australia
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Phone
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+61 3 9288 2549
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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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Prof Wayne Morrison
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Address
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St Vincents Hospital Melbourne
41 Victoria Pde
Fitzroy, VIC 3065
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Country
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Australia
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Phone
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+61 3 9288 2549
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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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