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Trial registered on ANZCTR
Registration number
ACTRN12613000122752
Ethics application status
Approved
Date submitted
25/01/2013
Date registered
1/02/2013
Date last updated
1/02/2013
Type of registration
Retrospectively registered
Titles & IDs
Public title
A New Test for Detecting Endometrial Cancer
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Scientific title
A New Test for Detecting Endometrial Cancer
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Secondary ID [1]
281823
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Nil Known
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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:
Endometrial Cancer
288173
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Condition category
Condition code
Cancer
288535
288535
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0
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Womb (Uterine or endometrial cancer)
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Participants admitted for treatment for endometrial cancer (usually involving a hysterectomy) undergo a uterine wash during the gynaecological procedure. The wash, which will take less than 5 minutes to collect, will contain enzymes called matrix metalloproteinases (MMPS), which are released into the uterine cavity in patients with endometrial cancer. Uterine washes will be transported to a test laboratory to be analysed for MMP levels using standard lab techniques. This testing will take a few hours to complete.
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Intervention code [1]
286375
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Early detection / Screening
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Comparator / control treatment
The control group is made up of participants who are known to not have endometrial cancer. These participants suffer from unrelated gynaecological conditions that still require them to undergo hysterctomy (ie prolapse). The uterine wash procedure and testing will be performed as that described for patients with endometrial cancer.
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Control group
Active
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Outcomes
Primary outcome [1]
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Detection of enodmetrial cancer through measurement of MMP biomarkers levels in uterine wash specimens.
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Assessment method [1]
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Timepoint [1]
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The effectiveness of the test will be determined at the end of the study.
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Primary outcome [2]
288766
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To determine the type of MMPs released into the uterine cavity of women with endometrial cancer and in women with other gynecological conditions.
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Assessment method [2]
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Timepoint [2]
288766
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The profiles of MMPs will be determined throughout and at the conclusion of the study.
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Secondary outcome [1]
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N/A
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Assessment method [1]
300776
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Timepoint [1]
300776
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N/A
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Eligibility
Key inclusion criteria
Peri-menopausal and post-menopausal women with endometrial cancer that are undergoing a hysterectomy procedure
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Minimum age
45
Years
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Maximum age
80
Years
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Sex
Females
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Can healthy volunteers participate?
No
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Key exclusion criteria
- Men
- Women who do not have endometiral cancer who do not fit the age range
- Women who are not already having non-cancer gynecological treatment
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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)
Patients enrolled as they present to Royal Women's Hospital that are eligible for the study
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people analysing the results/data
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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
Efficacy
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Statistical methods / analysis
NA
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Recruitment
Recruitment status
Suspended
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Date of first participant enrolment
Anticipated
7/03/2012
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Actual
7/03/2012
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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
20
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
VIC
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Recruitment hospital [1]
464
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The Royal Women's Hospital - Parkville
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Recruitment postcode(s) [1]
6215
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3052 - Parkville
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Funding & Sponsors
Funding source category [1]
286611
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Commercial sector/Industry
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Name [1]
286611
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Diagnotech Pty Ltd
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Address [1]
286611
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Level 34
360 Collins St
Melbourne VIC 3000
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Country [1]
286611
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Australia
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Primary sponsor type
Commercial sector/Industry
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Name
Diagnotech Pty Ltd
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Address
Level 34
360 Collins St
Melbourne VIC 3000
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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]
285398
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None
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Address [1]
285398
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None
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Country [1]
285398
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
The main aim of this study is to assess the ability of a new test to detect endometrial cancer in post-menopausal women. The diagnostic test being evaluated involves performing a wash of the uterus and collecting this wash fluid for analysis of markers that are shed from cancer cells. Two different laboratory testing methods will be used to obtain information that will enable us to develop a more cost-effective, sensitive and specific test for detecting early stages of endometrial cancer. Who is it for? This studyis open to peri- and post-menopausal women aged 45-80 years with endometrial cancer and who are currently undergoing a hystrectomy procedure. Trial details In this study you will undergo a uterine wash procedure while under general anesthetic prior to hysterectomy procedure. The wash sample is then tested for specific MMPs.
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Trial website
N/A
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Trial related presentations / publications
N/A
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Public notes
N/A
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Contacts
Principal investigator
Name
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Prof Michael Quinn
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Address
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Royal Women’s Hospital
Cnr Flemington Rd & Grattan St
Parkville VIC
3052
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Country
37246
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Australia
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Phone
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+61 3 93445188
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Fax
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Email
37246
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[email protected]
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Contact person for public queries
Name
37247
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Sacha Dopheide
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Address
37247
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81-89 Cotham Rd
Kew, Victoria
3101
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Country
37247
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Australia
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Phone
37247
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+61 3 99457527
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Fax
37247
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Email
37247
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[email protected]
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Contact person for scientific queries
Name
37248
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Sacha Dopheide
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Address
37248
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81-89 Cotham Rd
Kew, Victoria
3101
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Country
37248
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Australia
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Phone
37248
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+61 3 99457527
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Fax
37248
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Email
37248
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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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