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Trial registered on ANZCTR
Registration number
ACTRN12605000612617
Ethics application status
Approved
Date submitted
10/08/2005
Date registered
6/10/2005
Date last updated
6/10/2005
Type of registration
Retrospectively registered
Titles & IDs
Public title
The effectiveness of dietry intervention in the management of women with faecal incontinence.
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Scientific title
The effectiveness of dietry intervention in the management of women with faecal incontinence.
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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:
Anal incontinence/ defecation dysfunction
744
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Condition category
Condition code
Diet and Nutrition
820
820
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0
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Normal oral and gastrointestinal development and function
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Cross over dietary intervention study looking at the effect of modified fibre on bowel function over a period of 12 weeks.
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Intervention code [1]
165
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None
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Comparator / control treatment
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Control group
Active
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Outcomes
Primary outcome [1]
1052
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Cleveland Clinic continence scores, with improvement of > 50%
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Assessment method [1]
1052
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Timepoint [1]
1052
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Measured at completion of 12 week dietary intervention.
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Secondary outcome [1]
1957
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VAS of patient satisfaction, SF 36, Anorectal Symptom Questionaire, QOL Faecal Incontinence, at completion of 12 week dietary intervention.
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Assessment method [1]
1957
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Timepoint [1]
1957
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Eligibility
Key inclusion criteria
Fecal incontinence. Concomitant pelvic floor dysfunction - vaginal prolapse or urinary incontinence may be included.
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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
Cultural or religious dietary requirements preclude from participationMedical disorders which require a specific diet eg. Coeliac disease, food allergyPresence of rectovaginal fistula.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Not concealed
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Computer generated table of random numbers. Blocking used in groups of four.
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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
Crossover
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Other design features
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Phase
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Type of endpoint/s
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
8/10/2004
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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
40
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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]
908
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Hospital
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Name [1]
908
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Royal Womens Hospital Urogynaecology unit
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Address [1]
908
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Country [1]
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Australia
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Primary sponsor type
Hospital
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Name
Royal Womens Hospital Urogynaecology unit
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Address
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Country
Australia
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Secondary sponsor category [1]
767
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None
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Name [1]
767
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As above
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Address [1]
767
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Country [1]
767
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
2195
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Royal Womens hospital Melbourne
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Ethics committee address [1]
2195
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Ethics committee country [1]
2195
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Australia
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Date submitted for ethics approval [1]
2195
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Approval date [1]
2195
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Ethics approval number [1]
2195
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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
36394
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Address
36394
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Country
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Phone
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Fax
36394
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Email
36394
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Contact person for public queries
Name
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Dr Marcus Carey
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Address
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Urogynaecology Pelvic Floor Service
Grattan Street
Carlton VIC 3054
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Country
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Australia
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Phone
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+61 3 93442000
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Fax
9354
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Email
9354
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[email protected]
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Contact person for scientific queries
Name
282
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Kate Sloane
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Address
282
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Urogynaecology Pelvic Floor Service
Grattan Street
Carlton VIC 3054
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Country
282
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Australia
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Phone
282
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+61 3 93442000
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Fax
282
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Email
282
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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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