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Trial registered on ANZCTR
Registration number
ACTRN12619001250123
Ethics application status
Approved
Date submitted
10/04/2019
Date registered
10/09/2019
Date last updated
10/09/2019
Date data sharing statement initially provided
10/09/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Comparison between two different technique of applying fissure sealant on permenant molar teeth
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Scientific title
Evaluating the pit and fissure sealant retention capabilities of self-etch and conventional acid-etch techniques among school children aged between 8-10 year old: a clinical trial
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Secondary ID [1]
297933
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none
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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:
Non-cavitated teeth
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fully erupted tooth
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Condition category
Condition code
Oral and Gastrointestinal
311365
311365
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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
the Rationale of the experiment arm are:
-Finding on the use of (self-etch adhesives) which is the experiment arm is still inconclusive and further clinical trials are needed.
-There is no published clinical study employing a self-etch mode of universal adhesive agent for the placement of fissure sealants.
-With the elimination of the acid etching (rinsing and drying) steps (in the control arm), the need for fewer operative steps and shorter chair time is particularly interesting when treating paediatric patients
In the experiment arm, I will use dental material (not a drug) already in the market globally for more than 5 years (Single Bond Universal Adhesive Scotchbond™) as etching material in a self-etch way but the difference is that I will test the effectiveness of what the producer claims it's effective.
According to manufacturer instruction, the etching material will be raped on the tooth surface for 20 sec then blow with air and use the light cure.
All applications and examinations will be conducted by a single operator which is a dentist.
The self-etching material will be placed on the targeted molar just before the fissure sealant.
According to the pilot study we performed 5min is the estimated time for each tooth.
After curing the sealant will be checked for voids using an explorer.
The occlusion will be checked with articulation paper
The school children will be examined in their school as part of the local preventive program then the potential subject will be given participate sheet and consent form.
Then after that appointments will be arranged to apply the fissure sealant with a different technique in dental faculty um in optimal situations
then participants will be reviewed in 6 and 12 months later
Randomization between techniques will be achieved by computer-generated randomization
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Intervention code [1]
314157
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Prevention
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Comparator / control treatment
The golden stander technique in applying fissure sealant will be used as a control arm which known by an acid etch the tooth surface with 37% phosphoric acid for 30 sec. Then wash and dry without saliva contamination after that apply the fissure sealant which is the same in both arms (Clinpro TM Sealant, St Paul, MN, USA)
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Control group
Active
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Outcomes
Primary outcome [1]
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Primary outcome: Retention capability of fissure sealant
Evaluation criteria:
Using visual inspection to evaluate the sealants as described by Feigal RJ et al. (2000):
A) complete retention (all pits and fissures covered by the sealant)
B) partial loss (one or more fissures not covered by the sealant)
B1, without caries; B2, with caries
C) complete loss (all pits and fissures uncovered)
C1, without caries; C2, with caries
All follow up will be carried out by a single dentist.
There is no complications or possible adverse effects that may happen to your child
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Assessment method [1]
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Timepoint [1]
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6,9 and 12 months post-fissure sealant application.
6 months after fissure sealant applications is the primary timepoint.
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Secondary outcome [1]
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nill
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Assessment method [1]
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Timepoint [1]
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nill
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Eligibility
Key inclusion criteria
1. Children aged 8 to 10 years old
2. Sound and non-cavitated (ICDAS oA )occlusal surfaces of the first permanent molar
3. Fully erupted first permanent molars
4. Gained consent from each subject
5. Cooperative children
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Minimum age
8
Years
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Maximum age
10
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
1. Children below 8 years old and above 10 years old
2. Children with cavitated, previously placed restorations or sealants on their first permanent molars
3. No consent for treatment
4. Uncooperative children
5. Patients with parafunctional habits
6. Mentally challenged or physically handicapped
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Study design
Purpose of the study
Prevention
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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
Parallel
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Other design features
spilt mouth design
It is a popular design in oral health research, each of the two treatments (experiment and control) are randomly assigned to either the right or left halves of the dentition. So by this design, we can reduce the variables between the two groups.
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Phase
Not Applicable
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/11/2019
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Actual
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Date of last participant enrolment
Anticipated
30/11/2019
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Actual
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Date of last data collection
Anticipated
30/11/2020
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Actual
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Sample size
Target
160
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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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Malaysia
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State/province [1]
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KUALA LUMPUR
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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university of Malaya
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Address [1]
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Jalan Universiti, 50603 Kuala Lumpur, Wilayah Persekutuan Kuala Lumpur
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Country [1]
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Malaysia
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Primary sponsor type
Individual
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Name
yazeed magbul althomali
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Address
Depart. of paediatric dentistry & Orthodontics
faculty of dentistry, University of Malaya, 50603 Kuala Lumpur
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Country
Malaysia
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Secondary sponsor category [1]
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Individual
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Name [1]
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prof. Dr. sabri mousa
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Address [1]
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Depart. of paediatric dentistry & Orthodontics
faculty of dentistry, University of Malaya, 50603 Kuala Lumpur
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Country [1]
302350
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Malaysia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Medical Ethics Committee faculty of dentistry University of Malaya
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Ethics committee address [1]
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Faculty of Dentistry, University of Malaya, 50603 Kuala Lumpur
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Ethics committee country [1]
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Malaysia
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Date submitted for ethics approval [1]
303117
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Approval date [1]
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03/08/2018
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Ethics approval number [1]
303117
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Summary
Brief summary
In the intervention group, I will use dental material (not a drug) already in the market globally for more than 5 years (Single Bond Universal Adhesive Scotchbond™) but the difference is that I will test the effectiveness of what the producer claims it's effective. Study purpose This study is important to determine the superiority of retention clinically between the two techniques of sealant applications. Hypothesis There is a difference in sealant retention after the application of the self-etch (intervention) or the traditional acid-etch(control) techniques.
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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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Dr Yazeed Magbul althomali
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Address
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Depart. of Paediatric Dentistry & Orthodontics
Faculty of Dentistry, University of Malaya, 50603 Kuala Lumpur
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Country
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Malaysia
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Phone
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+60145231990
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Fax
92538
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Email
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[email protected]
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Contact person for public queries
Name
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Yazeed Magbul althomali
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Address
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Depart. of Paediatric Dentistry & Orthodontics
Faculty of Dentistry, University of Malaya, 50603 Kuala Lumpur
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Country
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Malaysia
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Phone
92539
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+60145231990
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Fax
92539
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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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Yazeed Magbul althomali
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Address
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Depart. of Paediatric Dentistry & Orthodontics
Faculty of Dentistry, University of Malaya, 50603 Kuala Lumpur
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Country
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Malaysia
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Phone
92540
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+60145231990
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Fax
92540
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Email
92540
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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
Doc. No.
Type
Citation
Link
Email
Other Details
Attachment
1831
Informed consent form
377370-(Uploaded-10-04-2019-02-47-45)-Study-related document.pdf
1832
Ethical approval
377370-(Uploaded-10-04-2019-02-49-04)-Study-related document.pdf
1833
Other
ministery of education approval
377370-(Uploaded-10-04-2019-02-53-09)-Study-related document.pdf
Results publications and other study-related documents
Documents added manually
Type
Is Peer Reviewed?
DOI
Citations or Other Details
Attachment
Basic results
No
377370-(Uploaded-19-05-2021-12-37-08)-Basic results summary.docx
Documents added automatically
No additional documents have been identified.
Download to PDF