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Trial registered on ANZCTR
Registration number
ACTRN12605000182695
Ethics application status
Approved
Date submitted
9/08/2005
Date registered
19/08/2005
Date last updated
15/12/2015
Type of registration
Retrospectively registered
Titles & IDs
Public title
Using the Gynecare MoniTorr* device to measure urethral pressure before incontinence surgery
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Scientific title
The measurement of urethral pressure with the MoniTORR* device to predict outcome after urinary incontinence surgery based on urodynamics studies at 6 months.
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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:
Urethral pressure
278
0
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Condition category
Condition code
Renal and Urogenital
314
314
0
0
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Other renal and urogenital disorders
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Surgery
315
315
0
0
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Other surgery
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Intervention/exposure
Study type
Observational
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Patient registry
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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
Urethral retro-resistance pressure (URP)measurement.
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Intervention code [1]
146
0
Diagnosis / Prognosis
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
368
0
Urodynamic stress incontinence
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Assessment method [1]
368
0
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Timepoint [1]
368
0
At 6 months after surgery
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Secondary outcome [1]
824
0
Visual analogue scale of patient satisfaction
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Assessment method [1]
824
0
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Timepoint [1]
824
0
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Secondary outcome [2]
825
0
Bladder diary
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Assessment method [2]
825
0
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Timepoint [2]
825
0
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Eligibility
Key inclusion criteria
Women with urodynamics stress incontinence undergoing a TVT procedure at the two study centres. Concomitant prolapse surgery is not a contraindication. Willingness to participate.
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Minimum age
Not stated
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Maximum age
Not stated
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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
Medically unfit for surgery. Refusal to participate. Patients who are recommended surgery other than TVT (e.g. Colposuspension, Sling, Bulking agent, Transobturator procedure).
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Study design
Purpose
Screening
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Duration
Longitudinal
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Selection
Defined population
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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
24/04/2005
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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
120
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Funding & Sponsors
Funding source category [1]
371
0
Commercial sector/Industry
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Name [1]
371
0
Johnson & Johnson Medical
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Address [1]
371
0
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Country [1]
371
0
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Primary sponsor type
Commercial sector/Industry
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Name
Johnson & Johnson Medical
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Address
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Country
United States of America
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Secondary sponsor category [1]
294
0
None
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Name [1]
294
0
n/a
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Address [1]
294
0
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Country [1]
294
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
1361
0
Royal Women's Hospital Human Ethics Committee
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Ethics committee address [1]
1361
0
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Ethics committee country [1]
1361
0
Australia
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Date submitted for ethics approval [1]
1361
0
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Approval date [1]
1361
0
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Ethics approval number [1]
1361
0
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Summary
Brief summary
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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
35779
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Address
35779
0
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Country
35779
0
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Phone
35779
0
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Fax
35779
0
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Email
35779
0
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Contact person for public queries
Name
9335
0
Dr Marcus Carey
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Address
9335
0
Frances Perry House
Suite D Level 10
Cardigan St
Carlton VIC 3053
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Country
9335
0
Australia
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Phone
9335
0
+61 3 92215099
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Fax
9335
0
+61 3 92215299
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Email
9335
0
[email protected]
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Contact person for scientific queries
Name
263
0
Dr Peta Higgs
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Address
263
0
Urogynaecology Department
Royal Women's Hospital
Grattan St
Carlton VIC 3053
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Country
263
0
Australia
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Phone
263
0
+61 3 93442000
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Fax
263
0
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Email
263
0
[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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