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Trial registered on ANZCTR
Registration number
ACTRN12619000517178
Ethics application status
Approved
Date submitted
9/03/2019
Date registered
1/04/2019
Date last updated
13/04/2024
Date data sharing statement initially provided
1/04/2019
Date results provided
1/03/2023
Type of registration
Prospectively registered
Titles & IDs
Public title
Feasibility of Water irrigation following resection of bladder tumour
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Scientific title
WATIP: Water Irrigation following transurethral resection of bladder tumour - a pilot study of feasibility and safety
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Secondary ID [1]
297682
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None
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Universal Trial Number (UTN)
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Trial acronym
WATIP
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Bladder Cancer
311960
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Condition category
Condition code
Cancer
310538
310538
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0
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Bladder
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Irrigation of the bladder using water irrigation during (by the surgeon in the operating theatre) and after (by nursing staff on the ward) bladder tumour resection. Duration of water irrigation will be for at least 3 hours, and can continue for longer at the discretion of the treating clinician
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Intervention code [1]
313914
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Treatment: Other
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Feasibility, assessed as at least 90% of eligible participants being able to receive the study intervention
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Assessment method [1]
319400
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Timepoint [1]
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Immediate - within 24 hours of resection
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Secondary outcome [1]
368024
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Safety - assessed by the rate of adverse events of CTCAE grade 3 or higher
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Assessment method [1]
368024
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Timepoint [1]
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24 to 48 hours following bladder tumour resection
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Secondary outcome [2]
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Recurrence-free survival
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Assessment method [2]
368025
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Timepoint [2]
368025
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3 and 12 months following bladder tumour resection
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Eligibility
Key inclusion criteria
1. Age 18 or older
2. Capacity to provide informed consent
3. Suspected bladder cancer on flexible cystoscopy or imaging
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Minimum age
18
Years
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Maximum age
No limit
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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
1. At risk of water toxicity:
a. History of hyponatraemia (serum sodium below normal limits, usually 135 mmol/L)
b. Chronic renal impairment (eGFR < 30)
c. Congestive cardiac failure (Ejection Fraction < 25%)
2. Suspected or confirmed pregnancy
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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)
N/A
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
N/A
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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
Not Applicable
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Type of endpoint/s
Safety/efficacy
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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
1/04/2019
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Actual
1/07/2019
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Date of last participant enrolment
Anticipated
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Actual
15/11/2021
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Date of last data collection
Anticipated
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Actual
1/02/2023
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Sample size
Target
30
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Accrual to date
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Final
30
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
13350
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Box Hill Hospital - Box Hill
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Recruitment hospital [2]
13351
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Maroondah Hospital - Ringwood East
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Recruitment postcode(s) [1]
25949
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3128 - Box Hill
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Recruitment postcode(s) [2]
25950
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3135 - Ringwood East
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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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ANZUP trials group
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Address [1]
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Lifehouse, Level 6, 119-143 Missenden Road,
Camperdown NSW 2050
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Country [1]
302207
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Australia
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Primary sponsor type
University
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Name
Monash University
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Address
Level 2
5 Arnold Street
Box Hill
Victoria 3128
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Country
Australia
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Secondary sponsor category [1]
302057
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None
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Name [1]
302057
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Address [1]
302057
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Country [1]
302057
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
302886
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Eastern Health Human Research Ethics Committee
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Ethics committee address [1]
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Level 2, 5 Arnold Street Box Hill Victoria 3128
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Ethics committee country [1]
302886
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Australia
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Date submitted for ethics approval [1]
302886
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Approval date [1]
302886
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21/02/2019
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Ethics approval number [1]
302886
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E12-2018
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Summary
Brief summary
The purpose of this study is to determine if continuous irrigation of the bladder using sterile water for at least 3 hours is feasible and safe in bladder tumour resection. Who is it for? You may be eligible for this study if you are an adult who is suspected of having bladder cancer. Study details Standard surgery for bladder tumours involves irrigation of the bladder during and after the surgery using sterile saline (salt water). If you participate in this study, you will have sterile water used for this irrigation during and for at least 3 hours after surgery instead. If irrigation using water is found to be feasible and safe, it can then be assessed further to see if it can prevent the bladder cancer. from coming back. This could have a major impact on treating bladder cancer
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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 Shomik Sengupta
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Address
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Eastern Health Clinical School, Monash University
Level 2, 5 Arnold Street
Box Hill
Victoria 3128
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Country
91738
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Australia
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Phone
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+61 03 9094 9546
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Fax
91738
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Email
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[email protected]
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Contact person for public queries
Name
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Shomik Sengupta
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Address
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Eastern Health Clinical School, Monash University
Level 2, 5 Arnold Street
Box Hill
Victoria 3128
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Country
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Australia
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Phone
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+61 03 9094 9546
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Fax
91739
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Email
91739
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[email protected]
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Contact person for scientific queries
Name
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Shomik Sengupta
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Address
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Eastern Health Clinical School, Monash University
Level 2, 5 Arnold Street
Box Hill
Victoria 3128
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Country
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Australia
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Phone
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+61 03 9094 9546
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Fax
91740
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Email
91740
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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)?
Yes
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What data in particular will be shared?
all of the individual participant data collected during the trial, after de-identification
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When will data be available (start and end dates)?
Immediately following publication, no end date
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Available to whom?
only researchers who provide a methodologically sound proposal
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Available for what types of analyses?
only to achieve the aims in the approved proposal
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How or where can data be obtained?
equirement to sign data access agreement,
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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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