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Trial registered on ANZCTR
Registration number
ACTRN12610001076066
Ethics application status
Approved
Date submitted
8/07/2010
Date registered
7/12/2010
Date last updated
1/07/2019
Date data sharing statement initially provided
1/07/2019
Type of registration
Retrospectively registered
Titles & IDs
Public title
Repeat prostate evaluation and therapy pilot study in patients undergoing high dose rate brachytherapy for prostate cancer
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Scientific title
A pilot study to evaluate tolerance, safety and efficacy of repeated prostate biopsy in patients undergoing high dose rate brachytherapy for prostate cancer
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Secondary ID [1]
252182
0
Peter MacCallum Cancer Centre 10-68
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Secondary ID [2]
253241
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PMCC 10/68
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Universal Trial Number (UTN)
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Trial acronym
RePEAT Pilot
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Prostate Cancer
257721
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Condition category
Condition code
Cancer
257890
257890
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0
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Prostate
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Repeated prostate biopsies are to be obtained from malignant areas identified on previous transrectal ultrasound biopsy. These will be prior to the first high dose rate (HDR) brachytherapy fractions and at various durations prior to the second HDR dose, and again approximately 30 minutes after that dose (i.e. up to 5 biopsies in total).
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Intervention code [1]
256774
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Treatment: Other
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Comparator / control treatment
NA
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
258755
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Unacceptable Toxicity Rate - a composite measure of infection (requiring >5 days of antibiotics), patient tolerance (refusal of subsequent biopsy) and grade 3 toxicity (using NCI CTC criteria)
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Assessment method [1]
258755
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Timepoint [1]
258755
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6 weeks following intervention completion
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Secondary outcome [1]
266472
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presence of prostate tissue on each biopsy assessed using light microscopy
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Assessment method [1]
266472
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Timepoint [1]
266472
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6 weeks following intervention completion
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Eligibility
Key inclusion criteria
Patients undergoing high dose rate brachytherapy for prostate cancer
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Minimum age
40
Years
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Maximum age
80
Years
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Sex
Males
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Can healthy volunteers participate?
No
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Key exclusion criteria
previous transurethral resection of prostate (TURP), anticoagulation, previous sepsis from prostate biopsy
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Study design
Purpose of the study
Diagnosis
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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
Completed
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Date of first participant enrolment
Anticipated
1/09/2010
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Actual
16/11/2010
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Date of last participant enrolment
Anticipated
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Actual
21/01/2014
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Date of last data collection
Anticipated
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Actual
21/06/2015
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Sample size
Target
13
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Accrual to date
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Final
32
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Recruitment in Australia
Recruitment state(s)
VIC
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Funding & Sponsors
Funding source category [1]
257265
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Charities/Societies/Foundations
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Name [1]
257265
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Prostate Cancer Foundation of America (PCF)
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Address [1]
257265
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Prostate Cancer Foundation
1250 Fourth Street
Santa Monica, CA 90401
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Country [1]
257265
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United States of America
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Primary sponsor type
Hospital
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Name
Peter MacCallum Cancer Centre
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Address
St Andrews Pl
E Melbourne
VIC 3000
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Country
Australia
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Secondary sponsor category [1]
256509
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None
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Name [1]
256509
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NA
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Address [1]
256509
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NA
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Country [1]
256509
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
259285
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Peter MacCallum Cancer Centre
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Ethics committee address [1]
259285
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St Andrew Pl E Melbourne VIC 3000
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Ethics committee country [1]
259285
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Australia
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Date submitted for ethics approval [1]
259285
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06/08/2010
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Approval date [1]
259285
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11/10/2010
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Ethics approval number [1]
259285
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10/68
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Summary
Brief summary
a preliminary study of the ability to obtain tissue before and after radiation therapy (using brachytherapy) for the purpose of studying the molecular and cellular response of the cancer.
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Trial website
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Trial related presentations / publications
none
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Public notes
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Contacts
Principal investigator
Name
31377
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Address
31377
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Country
31377
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Phone
31377
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Fax
31377
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Email
31377
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Contact person for public queries
Name
14624
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Scott Williams
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Address
14624
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Peter MacCallum Cancer Centre
St Andrews Place
E Melbourne
VIC 3000
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Country
14624
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Australia
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Phone
14624
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+61 3 9656 1111
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Fax
14624
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+61 3 9656 1424
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Email
14624
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[email protected]
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Contact person for scientific queries
Name
5552
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Scott Williams
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Address
5552
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Peter MacCallum Cancer Centre
St Andrews Place
E Melbourne
VIC 3000
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Country
5552
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Australia
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Phone
5552
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+61 3 9656 1111
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Fax
5552
0
+61 3 9656 1424
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Email
5552
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
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No/undecided IPD sharing reason/comment
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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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