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Trial registered on ANZCTR
Registration number
ACTRN12608000519358
Ethics application status
Approved
Date submitted
15/09/2008
Date registered
3/10/2008
Date last updated
4/07/2012
Type of registration
Retrospectively registered
Titles & IDs
Public title
Identification of Protein markers in ovarian cancer
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Scientific title
Identification Of Protein Markers Suitable for the early detection of ovarian cancer
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Secondary ID [1]
717
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Nil
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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:
Ovarian Cancer
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Condition category
Condition code
Cancer
3853
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Ovarian and primary peritoneal
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
All patients undergoing this study will be having an oophorectomy or hysterectomy for a gynecological malignancy or benign condition. The participants will be requested to donate biological samples: blood , tissue, ascites,urine and uterine lavage which does not interfere with other diagnostic tests, nor does it interfere with medical or surgical treatment required. Surgery will be performed in exactly same way, as if the biological samples had not been collected.
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Intervention code [1]
3401
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Early detection / Screening
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Comparator / control treatment
Not Applicable
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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To measure the different protein levels in ovarian cancer tissue, urine, plasma and uterine lavage. Advanced proteiomic method will be use to identify cancer specific proteins from the collected specimens
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Assessment method [1]
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Timepoint [1]
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Specimens will be collected and will be stored untill 500 participants are recruited and than specimens will be processed
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Primary outcome [2]
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Identification of cancer-specific protein markers for the early detection of Ovarian Cancer
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Assessment method [2]
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Timepoint [2]
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End of the data anlysis phase
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Secondary outcome [1]
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None
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Assessment method [1]
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Timepoint [1]
8033
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None
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Eligibility
Key inclusion criteria
Patients who have known Ovarian cancer diagnosed from a previous pathology specimen OR Patients with an Ovarian mass which may be beningn or malignat.
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Minimum age
18
Years
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Maximum age
90
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Inability to give consent
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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
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
Recruiting
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Date of first participant enrolment
Anticipated
1/09/2008
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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
100
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,VIC
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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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Ovarian Cancer Research Foundation
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Address [1]
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TOK Corporate Centre
Suite 2B
Level 1
459 Toorak Road
Toorak Vic 3142
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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
Ovarian cancer research fund
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Address
TOK Corporate Centre
Suite 2B
Level 1
459 Toorak Road
Toorak Vic 3142
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
3472
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Sydney South West Area Health Service ERC (Royal Prince Alfred Hospital)
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Ethics committee address [1]
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Royal Prince Alfred Hospital Building 92, Level 3 Missenden Road Campberdown NSW 2050
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
5921
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Approval date [1]
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28/08/2008
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Ethics approval number [1]
5921
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x08-0158
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Summary
Brief summary
This study aims to identify protein markers that are suitable for allowing early detection of ovarian cancer. Who is it for? You can join this study if you have either: (1) known ovarian cancer diagnosed from a previous pathology specimen. (2) an ovarian mass which may be benign or malignant. and you will be having surgical removal of either your ovary or ovaries (oophorectomy or ovariectomy) or your uterus (hysterectomy). Trial details: Participants will be requested to donate biological samples: blood, tissue, ascites (peritoneal cavity fluid), urine and uterine lavage (washings). This does not interfere with other diagnostic tests, or with the required medical or surgical treatment. Surgery will be performed in exactly same way, as if the samples had not been collected. Detection of ovarian cancer at its earliest stages provides a good prognosis for full recovery; however survival diminishes greatly when the cancer spreads beyond the ovary. Current ovarian cancer markers lack the accuracy needed to provide a suitable early detection test. This study uses new procedures to identify a number of candidate blood protein markers produced by ovarian cancers which may be suitable as early cancer markers.
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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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Dr. Philip Beale
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Address
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Royal Prince Alfred Hospital [RPAH]
Sydney Cancer Centre
Level 6 Gloucester House
Missenden Road
Camperdown
NSW 2050
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Country
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Australia
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Phone
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02 9515 6183
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Fax
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02 9515 5063
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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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Dr. Philip Beale
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Address
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Royal Prince Alfred Hospital [RPAH]
Sydney Cancer Centre
Level 6 Gloucester house
Missenden road
Camperdown
NSW 2050
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Country
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Australia
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Phone
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02 9515 6183
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Fax
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02 9515 5063
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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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