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Trial registered on ANZCTR
Registration number
ACTRN12613000877785
Ethics application status
Not yet submitted
Date submitted
31/07/2013
Date registered
7/08/2013
Date last updated
7/08/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
The use of tissue expanders for breast reconstruction – what you put in is not always what you get out! A Pilot study of Tissue Expander fill and final volumes
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Scientific title
The use of tissue expanders for breast reconstruction – what you put in is not always what you get out! A Pilot study of Tissue Expander fill and final volumes in women undergoing breast reconstruction after mastectomy
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Secondary ID [1]
282940
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nil known
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Universal Trial Number (UTN)
U1111-1146-2138
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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:
Pilot study involving the volumes of tissue expanders used in breast cancer related reconstructive surgeries
289760
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Condition category
Condition code
Surgery
290100
290100
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0
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Surgical techniques
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Cancer
290131
290131
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0
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Breast
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Assessing the difference in the fill volumes inserted into a tissue expander and the final volumes on removal of the tissue expander. A descrepency has been noted that will effect the size of the second stage implant that is inserted into the sub-pectoral pocket and thus the cosmetic outcome.
Type of Tissue expanders studied: 133MV Allergan style tissue expanders
The tissue expander is assessed at the time of second stage reconstruction which is usually anywhere between 3-4 months after the initial insertion.
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Intervention code [1]
287665
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Not applicable
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Comparator / control treatment
no control used
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
290141
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Difference in the volumes noted effect the size of the implant that is inserted into the sub-pectoral pocket. Surgeons should be aware of this descrepency and have a wide range of implant sizes available at the time of the second stage reconstructive surgery.
The fill volume is based on the total amount of normal saline inserted into the tissue expanders by the surgeon (intra-operatively at the 1st stage and at office based insertions
The final volume is measured in 2 ways; by volume displacement by placing the removed TE into a graduated beaker containing 500ml of fluid as well by weighing the TE itself.
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Assessment method [1]
290141
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Timepoint [1]
290141
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This is a pilot study of 32 tissue expanders evaluated in a 6 month period. An extension is planned.
Volume is measured at the time of the second stage implant reconstruction
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Secondary outcome [1]
304008
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The fill volume is based on the total amount of normal saline inserted into the tissue expanders by the surgeon (intra-operatively at the 1st stage and at office based insertions
The final volume is measured in 2 ways; by volume displacement by placing the removed TE into a graduated beaker containing 500ml of fluid as well by weighing the TE itself.
To postulate the cause of this decrepency - we assessed the biochemistry of the fluid within the tissue expanders at the 2nd stage surgery to determine if there was ingress of plasma into the normal saline that was inserted and we did find small amounts of plasma constituents; this points towards a defect in the valves. Other investigators have also assessed the valve mechanisms, osmotic gradients across the membranes and colloid osmotic swelling.
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Assessment method [1]
304008
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Timepoint [1]
304008
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6 months
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Eligibility
Key inclusion criteria
All patients undergoing Tissue expander/Implant based breast reconstruction after mastectomy - 6 month period in 2012
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Minimum age
No limit
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Ruptured/leaking tissue expanders
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Convenience sample
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Timing
Prospective
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Statistical methods / analysis
Data was collected in an Excel 2010 workbook and analysed using NCSS software. A paired t-test was used to compare volumes and a p value of <0.05 considered significant.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/02/2012
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Actual
14/02/2012
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Date of last participant enrolment
Anticipated
31/07/2012
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Actual
25/07/2012
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
32
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
1369
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Sir Charles Gairdner Hospital - Nedlands
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Recruitment hospital [2]
1370
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Mount Hospital - Perth
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Recruitment postcode(s) [1]
7231
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6009 - Broadway Nedlands
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Funding & Sponsors
Funding source category [1]
287716
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Self funded/Unfunded
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Name [1]
287716
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no funding was required
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Address [1]
287716
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not applicable
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Country [1]
287716
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Primary sponsor type
Individual
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Name
Dr Ananda Kallyani S M Ponniah
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Address
Breast Centre
Sir Charles Gairdner Hospital
Hospital Avenue
Nedlands 6009
Western Australia
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Country
Australia
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Secondary sponsor category [1]
286446
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None
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Name [1]
286446
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Address [1]
286446
0
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Country [1]
286446
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Ethics approval
Ethics application status
Not yet submitted
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Ethics committee name [1]
289672
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Ethics Comittee/unit
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Ethics committee address [1]
289672
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Sir Charles Gairdner Hospital Hospital Avenue Nedlands 6009 Western Australia
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Ethics committee country [1]
289672
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Australia
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Date submitted for ethics approval [1]
289672
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30/07/2013
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Approval date [1]
289672
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Ethics approval number [1]
289672
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Summary
Brief summary
The primary purpose of this study is to evaluate tissue expander fill and final volumes in women undergoing breast reconstruction. Who is it for? This study included women who underwent tissue expander/implant based breast reconstruction following mastectomy. The surgeries were conducted over a 6 month period in 2012. Trial details All participants in this study underwent breast reconstruction surgery with tissue expander. The tissue expander fill volume inserted at the time of first implant was compared to the final volume on removal of the tissue expander at the time of second stage reconstructions (about 3-4 months later). A discrepancy between these values affects the size of the second stage implant and thus the cosmetic outcome.
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Trial website
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Trial related presentations / publications
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Public notes
As the study does not involve human or animal tissue a formal ethical approval may not be necessary; however the study has been referred to the ethical comittee in Sir Charles Gairdner Hospital and we are awaiting their feedback
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Contacts
Principal investigator
Name
41890
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Dr Ananda Kallyani S M Ponniah
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Address
41890
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The Breast Centre
Sir Charles Gairdner Hospital
Hospital Avenue
Nedlands 6009
WA
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Country
41890
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Australia
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Phone
41890
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+61405219079
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Fax
41890
0
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Email
41890
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[email protected]
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Contact person for public queries
Name
41891
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Ananda Kallyani S M Ponniah
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Address
41891
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The Breast Centre
Sir Charles Gairdner Hospital
Hospital Avenue
Nedlands 6009
WA
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Country
41891
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Australia
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Phone
41891
0
+61405219079
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Fax
41891
0
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Email
41891
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[email protected]
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Contact person for scientific queries
Name
41892
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Ananda Kallyani S M Ponniah
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Address
41892
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The Breast Centre
Sir Charles Gairdner Hospital
Hospital Avenue
Nedlands 6009
WA
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Country
41892
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Australia
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Phone
41892
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+61405219079
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Fax
41892
0
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Email
41892
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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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