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Trial registered on ANZCTR
Registration number
ACTRN12610000325000
Ethics application status
Approved
Date submitted
18/04/2010
Date registered
21/04/2010
Date last updated
1/12/2020
Date data sharing statement initially provided
17/07/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
A longitudinal study of caries development in children from 4 to 15 years of age
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Scientific title
A randomised phase III study to determine the longitudinal effects of chlorhexidine toothpaste and Casein Phosphopeptide- Amorphous Calcium Phosphate (CPP-ACP Tooth Mousse) in the treatment of dental caries in children to prevent new lesions
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Secondary ID [1]
251638
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"None"
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Universal Trial Number (UTN)
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Trial acronym
ECC 4-15
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
dental caries
257206
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Condition category
Condition code
Oral and Gastrointestinal
257349
257349
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0
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Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
This study is a continuation of study "A longitudinal study of caries prevention in children aged two to four years" ACTRN12609000330246 and will be recruiting participants who have already undergone and will continue to undergo two interventions arms. Either brushing teeth with fluoridated toothpaste in combination with CPP-ACP Tooth Mousse or brushing teeth with fluoridated toothpaste in combination with 0.12% chlorhexidine toothpaste from 4 years until 7 years of age.
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Intervention code [1]
256332
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Prevention
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Comparator / control treatment
Control group is toothbrushing daily with only fluoridated toothpaste
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Control group
Active
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Outcomes
Primary outcome [1]
258248
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Less numbers of carious lesions and or demineralised tooth surfaces as detected through visual examination.
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Assessment method [1]
258248
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Timepoint [1]
258248
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6 monthly starting when a child is 4.5 years of age and then once when they are 12 years of age and once when they are 15 years of age
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Primary outcome [2]
258249
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Less numbers of teeth with erosion as determined through visual examination.
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Assessment method [2]
258249
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Timepoint [2]
258249
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6 monthly starting when a child is 4.5 years of age and then once when they are 12 years of age and once when they are 15 years of age
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Secondary outcome [1]
263906
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Lower levels of decay causing bacteria as detected through Caries Risk Test (CRT) Bacteria Test by Ivoclar.
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Assessment method [1]
263906
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Timepoint [1]
263906
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6 monthly starting when a child is 4.5 years of age and then once when they are 12 years of age and once when they are 15 years of age
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Eligibility
Key inclusion criteria
All children who complete research study "A longitudinal study of caries prevention in children aged two to four years"
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Minimum age
4
Years
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Maximum age
15
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Children who are diagnosed with milk protein allergies will be removed from the intervention group of Tooth Mousse and continue the project in the Fluoride only group.
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Study design
Purpose of the study
Prevention
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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)
Continuation of previously randomised product use as per allocation by opaque envelopes
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Continuation of simple randomisation by using procedures such as coin tossing and dice rolling
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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
Parallel
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Other design features
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Phase
Phase 4
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Date of first participant enrolment
Anticipated
1/06/2010
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Actual
1/01/2011
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Date of last participant enrolment
Anticipated
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Actual
1/01/2013
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Date of last data collection
Anticipated
31/12/2027
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Actual
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Sample size
Target
2100
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Accrual to date
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Final
491
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Recruitment in Australia
Recruitment state(s)
QLD
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Recruitment postcode(s) [1]
2828
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4114
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Funding & Sponsors
Funding source category [1]
256836
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Government body
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Name [1]
256836
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Metro South Health Service District, Oral Health Program, Logan Beaudesert Division
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Address [1]
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Kingston Oral Health Centre, Juers St Kingston, Qld 4114
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Country [1]
256836
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Australia
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Primary sponsor type
Government body
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Name
Metro South Health Service District, Oral Health Program, Logan Beaudesert Division
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Address
Kingston Oral Health Centre, Juers St Kingston, Qld 4114
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Country
Australia
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Secondary sponsor category [1]
256111
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None
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Name [1]
256111
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Address [1]
256111
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Country [1]
256111
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
258853
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Metro South Health Service District (HSD) Human Research Ethics Committee (HREC)
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Ethics committee address [1]
258853
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Level 2, Building 35, Princess Alexandra Hospital, Ipswich Road, Woolloongabba, QLD 4102
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Ethics committee country [1]
258853
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Australia
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Date submitted for ethics approval [1]
258853
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10/05/2010
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Approval date [1]
258853
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13/10/2010
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Ethics approval number [1]
258853
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Ethics committee name [2]
300662
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The University of Queensland Dental Sciences Research Ethics Committee
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Ethics committee address [2]
300662
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200 Turbot St Brisbane Queensland 4000
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Ethics committee country [2]
300662
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Australia
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Date submitted for ethics approval [2]
300662
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11/11/2010
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Approval date [2]
300662
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02/12/2010
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Ethics approval number [2]
300662
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1014
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Summary
Brief summary
In this study we will continue to follow participants recruited to " A longitudinal study of caries prevention in children aged two to four years" HREC/09/QPAH/158, ACTRN12609000330246 who have undergone preventative methods of education, home visits and toothbrushing with fluoride toothpaste, 0.12% chlorhexideine gel and CPP-ACP Tooth Mousse. The effectiveness of these strategies will be assessed through -microbial analysis for the presence of decay causing bacteria - clinical dental examination data - statistical analysis of data for case and control groups
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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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Ms Leigh Harrison-Barry
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Address
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Metro South Oral Health, 228 Logan Road, Woolloongabba, QLD, 4102
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Country
31070
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Australia
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Phone
31070
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+617 33171481
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Fax
31070
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+617 33171499
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Email
31070
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[email protected]
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Contact person for public queries
Name
14317
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Leigh Harrison-Barry
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Address
14317
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Metro South Oral Health, 228 Logan Road, Woolloongabba, QLD, 4102
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Country
14317
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Australia
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Phone
14317
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+617 33171481
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Fax
14317
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+617 33171499
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Email
14317
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[email protected]
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Contact person for scientific queries
Name
5245
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Leigh Harrison-Barry
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Address
5245
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Metro South Oral Health, 228 Logan Road, Woolloongabba, QLD, 4102
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Country
5245
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Australia
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Phone
5245
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+617 33171481
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Fax
5245
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+617 33171499
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Email
5245
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
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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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