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Trial registered on ANZCTR
Registration number
ACTRN12610000878077
Ethics application status
Not yet submitted
Date submitted
16/10/2010
Date registered
19/10/2010
Date last updated
19/10/2010
Type of registration
Retrospectively registered
Titles & IDs
Public title
Microtip and 7-channel catheter for urethral pressure measurements: a prospective comparative study
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Scientific title
Measuring the human urethral pressure with the standard Microtip catheter and the new 7-channel catheter and assessment of agreement of the two catheters in a prospective comparative study
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Secondary ID [1]
252885
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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:
Physiological urethral pressure in healthy human volunteers
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Condition category
Condition code
Renal and Urogenital
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0
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Normal development and function of male and female renal and urogenital system
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The urethral pressure is measured with the standard urethral pressure catheter Microtip. After this measurement the urethral pressure is measured again with the new 7-channel catheter. The intervention is a part of a urodynamic evaluation for which the women are scheduled. Each measurement is taken once in each patient.
The microtip catheter is has 2 sensors (one in the bladder, one in the urethra) and is withdrawn through the urethra using a mechanical puller at a constant speed. Measurement take about 1 minute.
The 7-channel catheter has 7 individual sensors at 5 mm distance between each of them, size 8 French, flexible. It is not withdrawn. Measurement take about 1 minute.
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Intervention code [1]
257413
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Diagnosis / Prognosis
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Comparator / control treatment
The control of the new 7-channel catheter is the standard Microtip catheter.
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Control group
Active
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Outcomes
Primary outcome [1]
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Urethral pressure measured in cmH20.
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Assessment method [1]
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Timepoint [1]
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At the measurement. There is only one measurement.
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Secondary outcome [1]
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Adverse events:
- pains: pains are assessed by questioning (visual analogue scale VAS).
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Assessment method [1]
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Timepoint [1]
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- pains: assessment before, during and immediately after the procedure.
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Eligibility
Key inclusion criteria
A continuous series of women scheduled for a urodynamic evaluation.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Urinary tract infection.
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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
Completed
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Date of first participant enrolment
Anticipated
1/01/2003
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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
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Actual
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Sample size
Target
21
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
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Switzerland
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State/province [1]
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Funding & Sponsors
Funding source category [1]
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Hospital
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Name [1]
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Department of Urology, University of Bern
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Address [1]
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Inselspital
Anna Seiler-Haus
CH-3010 Bern
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Country [1]
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Switzerland
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Primary sponsor type
Hospital
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Name
Department of Urology, University of Bern
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Address
Inselspital
Anna Seiler-Haus
CH-3010 Bern
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Country
Switzerland
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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]
257082
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Ethics approval
Ethics application status
Not yet submitted
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Summary
Brief summary
This study has not been judged by an official ethics committee, which has a HREC Number. At this time around 2002, this kind of small studies was discussed and ethically judged and eventually approved by the staff of the Department of Urology, University of Bern. The purpose of this study was to compare the standard microtip catheter with the new 7-channel catheter in terms of accuracy and safety measuring the urethral pressure. Both measurements are very similar, easy to do and non-invasive. The catheter in placed into the urethra, like a foley catheter. The hypothesis was, that the measurement with the 7-channel catheter was even accurate and less uncomfortable for patients, because it was not withdrawn. With about 1 minute both measurements were short. Based on the experience with the microtip catheter, no side effects, like pain, were expected
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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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Frederic Birkhaeuser
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Address
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Department of Urology
Inselspital
Anna Seiler-Haus
CH-3010 Bern
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Country
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Switzerland
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Phone
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+41 31 632 36 41
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Fax
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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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Frederic Birkhaeuser
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Address
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Department of Urology
Inselspital
Anna Seiler-Haus
CH-3010 Bern
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Country
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Switzerland
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Phone
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+41 31 632 36 41
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Fax
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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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