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Trial registered on ANZCTR
Registration number
ACTRN12621000329864
Ethics application status
Approved
Date submitted
15/02/2021
Date registered
23/03/2021
Date last updated
23/03/2021
Date data sharing statement initially provided
23/03/2021
Type of registration
Retrospectively registered
Titles & IDs
Public title
Does Confocal Laser Endomicroscopy enable identification of positive and negative surgical margin during breast cancer surgery.
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Scientific title
Does Confocal Laser Endomicroscopy enable identification of positive and negative surgical margin during breast conservation surgery (wide local excision and cavity shave).
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Secondary ID [1]
303457
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TGA clinical trial notification CT-2020-CTN-03062-1 V1
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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:
Cancer
320765
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Condition category
Condition code
Cancer
318594
318594
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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
Tissue excised during wide local excision with cavity shaves will be stained with acriflavine and then imaged intraoperatively with a handheld confocal endomicroscope, with images being collected and assessed for involved margins for each piece of tissue excised during the procedure. Tissue will then be fixed and processed using standard pathology processes. The ability of confocal endomicroscopy to identify involved margins will be assessed against the results from pathology. The surgeon and pathologists will be blinded to the confocal imaging results, so there will be no deviation from normal standard of care for patients in this study.
The tissue will be excised as per standard of care before imaging.
The confocal endomicroscopy will be done by an Optiscan technician who is trained in the use of the endomicroscope.
This will not add any additional time to the surgical procedure as it is being performed on excised tissue.
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Intervention code [1]
319989
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Not applicable
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Comparator / control treatment
Standard pathology will be used as the reference comparator for this study. This involves the standard protocol for tissue cut-up, blocking, sectioning and placing onto glass slides followed by H&E staining and examination of the stained sections by a pathologist.
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Control group
Active
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Outcomes
Primary outcome [1]
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Accurate identification of positive cancer margins intraoperatively using a confocal endomicroscope. Accuracy of margin identification to be compared to standard pathology.
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Assessment method [1]
326552
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Timepoint [1]
326552
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Intraoperatively - within a few minutes of the tissue being excised.
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Primary outcome [2]
326833
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Accurate identification of negative cancer margins intraoperatively using a confocal endomicroscope. Accuracy of margin identification to be compared to standard pathology.
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Assessment method [2]
326833
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Timepoint [2]
326833
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Intraoperatively - within a few minutes of the tissue being excised.
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Secondary outcome [1]
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Nil
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Assessment method [1]
391852
0
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Timepoint [1]
391852
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Nil
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Eligibility
Key inclusion criteria
Patients over age 18 years with breast cancer undergoing primary wide local excision with cavity shave (“WLE + CS”)
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Minimum age
18
Years
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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
Patients undergoing re-excision after prior wide local excision (“WLE”).
Patients without study consent.
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Study design
Purpose
Natural history
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Duration
Cross-sectional
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Selection
Convenience sample
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Timing
Prospective
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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
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Actual
4/03/2021
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Date of last participant enrolment
Anticipated
14/05/2021
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Actual
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Date of last data collection
Anticipated
31/05/2021
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Actual
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Sample size
Target
20
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Accrual to date
2
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
18719
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Royal Melbourne Hospital - Royal Park campus - Parkville
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Recruitment hospital [2]
18720
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Frances Perry House - Parkville
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Recruitment hospital [3]
18721
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Epworth Freemasons (Clarendon Street) - East Melbourne
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Recruitment postcode(s) [1]
33162
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3052 - Parkville
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Recruitment postcode(s) [2]
33163
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3002 - East Melbourne
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Funding & Sponsors
Funding source category [1]
307875
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Other
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Name [1]
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Medical Device Partnering Program
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Address [1]
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c/o Swinburne University of Technology
Building EN, Level 6
John St, Hawthorn, Vic, 3122
Mail H39, PO Box 218
Hawthorn, Vic, 3122
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Country [1]
307875
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Australia
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Funding source category [2]
307878
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Commercial sector/Industry
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Name [2]
307878
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Optiscan Pty Ltd
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Address [2]
307878
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16 Miles St
Mulgrave, Vic, 3170
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Country [2]
307878
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Optiscan Pty Ltd
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Address
16 Miles St
Mulgrave, Vic 3170
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Country
Australia
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Secondary sponsor category [1]
308587
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None
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Name [1]
308587
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None
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Address [1]
308587
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None
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Country [1]
308587
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
307876
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Melbourne Health Human Research Ethics Committee
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Ethics committee address [1]
307876
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Office for Research The Royal Melbourne Hospital Level 2 South West 300 Grattan St Parkville Vic 3050 Australia
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Ethics committee country [1]
307876
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Australia
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Date submitted for ethics approval [1]
307876
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29/09/2020
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Approval date [1]
307876
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10/12/2020
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Ethics approval number [1]
307876
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HREC/68536/MH-2020
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Summary
Brief summary
The purpose of this study is to determine if an imaging method called confocal endomicroscopy can accurately identify the margins of breast cancer during surgery. Who is it for? You may be eligible for this study if you are an adult who has breast cancer and is undergoing primary wide local excision with cavity shave. Study details Participants in this study will undergo their usual treatment, meaning their primary wide local excision procedure. During this procedure the surgeon will take some cancerous tissue and perform the imaging test and then send the tissue for standard pathology tests. There will be no additional involvement from participants. If it is determined that confocal endomicroscopy can accurately determine the margins of breast cancer then it would lead to a larger study. It is hoped that the larger study will determine whether using confocal endomicroscopy during surgery can better define the surgical margin at the time of the operation and significantly reduce the likelihood of a second operation.
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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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Prof Bruce Mann
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Address
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Professor of Surgery, Director of Breast Service, Royal Melbourne and Royal Women’s Hospital.
Suite 12, The Royal Women's Hospital, Parkville, Victoria, 3052, Australia
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Country
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Australia
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Phone
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+61 3 93476301
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Fax
108782
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Email
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[email protected]
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Contact person for public queries
Name
108783
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Lindsay Bussau
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Address
108783
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Optiscan Pty Ltd
16 Miles St
Mulgrave, Vic, 3170
Australia
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Country
108783
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Australia
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Phone
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+61 417 227 107
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Fax
108783
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Email
108783
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[email protected]
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Contact person for scientific queries
Name
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Lindsay Bussau
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Address
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Optiscan Pty Ltd
16 Miles St
Mulgrave, Vic, 3170
Australia
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Country
108784
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Australia
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Phone
108784
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+61 417 227 107
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Fax
108784
0
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Email
108784
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
This is a small early stage study to determine if this technology can identify involved surgical margins intraoperatively. If successful, the findings of this study will help us better define how IPD can be shared in future studies.
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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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