Prevention of Dental CariesNCT06602765
Comparative Analysis of Interventions for Prevention of Dental Caries in School Children
A study testing Tooth brushing, tooth paste containing 1450ppm fluoride in people with Prevention of Dental Caries, run by Bahria University at 1 site in Pakistan.
Trial summary
A study aims to assess the most effective preventive interventions to address the widespread issue of dental caries, affecting an estimated 2 billion people in permanent teeth and over 500 million children in primary teeth globally. Notably, in Pakistan, over 90% of caries-affected teeth are untreated. Read more about this study
- Who is it for?
- Ages 6 to 7 yearsHealthy volunteers can take part
- Conditions the study is for
- Prevention of Dental Caries
- What is being tested?
- Tooth brushing, tooth paste containing 1450ppm fluoride
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 180 participants
- Where
- 1 sitePakistan
- Study dates
- 5 Oct 2024to 30 Nov 2025
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 6 to 7 years
- All sexes
- Healthy volunteers accepted
- Child
Who may be able to join
- Schoolchildren aged 6-7 years Sound 1st permanent molars Consent obtained from parents/guardians Cooperative Children
Who cannot join
- 1st Permanent molar has not erupted. Children with disability. Special Children (e.g. Down syndrome)
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Comparative Analysis of Interventions for Prevention of Dental Caries in School Children: A Randomized Controlled Trial
A study aims to assess the most effective preventive interventions to address the widespread issue of dental caries, affecting an estimated 2 billion people in permanent teeth and over 500 million children in primary teeth globally. Notably, in Pakistan, over 90% of caries-affected teeth are untreated. Despite schools being a platform for public health initiatives, there is limited evidence on oral health promotion in low and middle-income countries. This study compares different preventive strategies' effectiveness and cost-efficiency for caries prevention in schoolchildren.
The randomized controlled trial will occur in Naval Schools of Karachi under the Pakistan Navy Educational Trust (PNET) over one year, including intervention and follow-up periods. The interventions include a combination of fluoride toothpaste, dietary counselling, and fissure sealant application. A multi-stage sampling method will select schools and classes, while convenience random sampling will select 180 children for the study. A single-blind trial will be conducted, with the data analyst unaware of the intervention groups.
Read more
Participants will be divided into three groups. Group 1 (Control) will use fluoride toothpaste and be instructed to brush twice daily. Group 2 (Intervention-1) will receive 14500 ppm fluoride toothpaste and oral health education. Group 3 (Intervention-2) will include the treatments from Group 2 plus fissure sealants on the first permanent molars. Parents in Groups 2 and 3 will receive a standardized advice sheet to reinforce oral hygiene practices at home.
The study will collect baseline demographic data, including age, gender, socioeconomic status, family education, existing oral hygiene practices, dental knowledge, and dentition status. Oral examinations will be conducted according to international standards. Statistical analysis will employ Chi-Square, ANOVA, and logistic regression tests, with a significance level set at 0.05.
The study aims to determine the most effective preventive strategy by comparing the reduction in dental caries incidence across the groups. The findings will guide recommendations for implementing the most effective intervention on a larger scale in schools, with the goal of reducing the burden of dental caries in children.
Read the detailed description
Ethical Approval approved by the BUHSC ethical committee. School administrations will be approached for permission. Consent forms will be sent to the parents of the children before the data collection visit. The data collection team comprised of 06 members will visit the selected schools. A signed consent form will be taken, and verbal consent will be obtained from the children as well. The children fulfilling the inclusion criteria will be sequenced as a list. Randomization will be done through SNOSE - a sequential number of opaque sealed envelopes will be done, and the students will then be allocated in 3 groups.
PI, Co-PI, and 05 team members will conduct oral examinations in the selected schoolyard or inside a classroom, following the standard international guidelines (WHO 2013). In addition, the baseline demographic data will also be collected comprising of age, gender, socioeconomic status (SES), family education and existing oral hygiene practices, dental knowledge, and dentition status by the parents and participants. Group 1 (Control) will be given fluoride toothpaste containing 1450 ppm Fluoride and will be asked to brush at least twice daily with a pea-sized amount of toothpaste, using the modified bass technique. This will be considered as control. Some intervention in the control group will also address the ethical issues. Parents will be guided for the tooth brushing.
Group 2 (Intervention -1) will be given fluoride toothpaste containing 1450 ppm Fluoride and will be asked to brush at least twice daily with a pea-sized amount of toothpaste and oral health education. A modified bass technique for tooth brushing will be used. Oral health education through audio-visual aids, pamphlets, and live demonstrations on study models will cover proper tooth brushing techniques, the use of a good toothbrush, and healthy eating habits, including special emphasis on proteins and dairy products and alternate use of sugars in daily routine. E.g. soft drinks that are high in sugar can be replaced with drinking milk and water.
Group 3 (Intervention -1) will be given fissure sealants on 1st permanent molar along with the strategy given to Group 2. Fissure sealing compounds, Glass ionomer will be used on school children who will qualify for inclusion criteria. Mobile Dental Unit and fissure sealant kit will be taken to the site and children will be provided fissure sealant in their setting.
In the intervention group (2 and 3) parents will also be given an Evidence-Based standardized parental advice sheet to reinforce instructions at home.
The saliva of school children will be collected by spitting in a test tube. For children over the age of 6, saliva can be collected using the expectoration, or spit method. In this process, the child is instructed to keep their mouth closed for three minutes without swallowing, allowing saliva to accumulate before spitting it into a collection tube. However, some children may struggle with this technique due to the challenge of not swallowing for an extended period. An alternative method is the drainage technique. Here, the child is first asked to swallow their saliva to stimulate the production of more saliva. Then, with their lips slightly parted, the saliva is allowed to drain directly into the collection tube The samples will be taken to the laboratory within 02 hours of collection Streptococcus mutans count will be conducted on collected saliva at the first visit to provide an initial bacterial count as baseline data before intervention and after six-month and 12-month bacterial count after the intervention. The primary medium used to identify streptococci is Mitis-Salivarius agar or its variant with bacitracin (MSB). Additionally, saliva's pH, flow rate, and buffering capacity will be measured in the lab. The first visit will be followed by six months and 12 months respectively. A preliminary pilot study will be undertaken with a limited sample size to assess the practicality of the interventions and enhance the process of collecting data.
The data collected through the questionnaire and log book filled by parents at home will be computerized, followed by converting it into the appropriate SPSS files. The outcome variables for assessing dental caries will be measured by ICDAS. The ICDAS is a two-digit coding method. One for caries and the other for sealant and restorations. In this research, only the caries coding method will be used. For caries, the method ranges from sound teeth (code 0), through enamel caries lesions (codes 1-3), to carious lesions in dentine (codes 4-6). For sealant and restoration, the method ranges from 0 to 8 as follows: 0 = Sound, 1 = Sealant, partial, 2 = Sealant, full, 3 = Tooth-coloured restoration, 4 = Amalgam restoration, 5 = Stainless steel crown, 6 = Porcelain or gold or Porcelain-Fused-to-Metal (PFM) crown or veneer, 7 = Lost or broken restoration, 8 = Temporary restoration (will not be used). Caries Codes (0 = sound tooth surface; A = first visual change in enamel; B = distinct visual change in enamel; 3 = enamel breakdown, no dentine visible; 4 = dentinal shadow (not cavitated into dentine); 5 = distinct cavity with visible dentine; 6 = extensive distinct cavity with visible dentine); Missing Teeth (97 = extracted due to caries; 98 = missing for other reasons; 99 = un-erupted).
Salivary indicators i.e. salivary flux - 0.3-0.4 ml/min. Salivary pH - 5-5.8, high acidity; 6.0-6.6, moderate acidity; 6.8-7.8, normal salivary pH Salivary buffer capacity - 3-30 mg/100 ml. Salivary Mutans count - < 10^5 CFU/ml saliva or ≥ 10^5 CFU/ml saliva. The study will use the CONSORT checklist for reporting the randomized control trial.
- Conditions
- Prevention of Dental Caries
- Being tested
- Tooth brushing, tooth paste containing 1450ppm fluoride
- Keywords
- Fissure sealant, Fluoride, Caries, Saliva, Dietary counselling
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Tooth brushing, tooth paste containing 1450ppm fluorideOther
Also called dietary counselling, fissure sealent, Glassionomer cement
brushing with fluoride toothpaste, dietary counselling for caries prevention and application of fissure sealant compound on first permanent t molars.
| Study group | Role | What they receive |
|---|---|---|
| tooth-brushing | Active comparator | In Control arm, tooth brushing with fluoride toothpaste using pea-sized toothpaste, using bass technique. Receives: Other: Tooth brushing, tooth paste containing 1450ppm fluoride |
| tooth-brushing and dietary counselling | Active comparator | In intervention arm 1, tooth brushing with fluoride toothpaste using pea-sized toothpaste, using the bass technique, and dietary counselling. Receives: Other: Tooth brushing, tooth paste containing 1450ppm fluoride |
| tooth-brushing , dietary counselling and fissure sealing of 1st permanent molar | Active comparator | In the intervention arm 2, tooth brushing with fluoride toothpaste using pea-sized toothpaste, using the bass technique, dietary counseling, and application of fissure sealant on a permanent first molar. Receives: Other: Tooth brushing, tooth paste containing 1450ppm fluoride |
What is being measured
The primary outcome is the main question the study is designed to answer.
Prevention of dental Caries
Compare the effectiveness of the combination of different preventive strategies which include tooth brushing with fluoride toothpaste, dietary counselling, and fissure sealant application for reducing the incidence of dental caries among school children
Measured: 1 year
Secondary outcomes (2)
Dietary Analysis
Dietary analysis to understand the risk factors and mechanisms underlying dental caries development among school children
Measured: 1 year
Streptococcus mutans in Saliva
Determine the contribution of saliva tests for Streptococcus mutans presence
Measured: 1 year
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted19 Sep 2024
- Study start5 Oct 2024
- Primary completion5 Nov 2025 (estimated)
- Study completion30 Nov 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Prevention of Dental CariesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Control, Interventional group 1, Interventional group 2
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 180 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Bahria University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Kulsoom Rizvi, Bahria University
- Investigators
- Kulsoom F Rizvi, MSc, Principal investigator, Bahria University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06602765
- Sponsor's protocol ID
- BUHS-IRB#061/24
- Status last verified
- Sep 2025
- First submitted
- 21 Jul 2024
- Last updated
- 23 Sep 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 23 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparative Analysis of Interventions for Prevention of Dental Caries in School Children: A Randomized Controlled Trial
- ClinicalTrials.gov ID
- NCT06602765
- Acronym / sponsor ID
- BUHS-IRB#061/24
- Conditions
- Prevention of Dental Caries
- Keywords
- Fissure sealant, Fluoride, Caries, Saliva, Dietary counselling
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 180 participants (estimated)
- Lead sponsor
- Bahria UniversityUniversity, hospital or other
- Study start
- 5 Oct 2024 (actual)
- Primary completion
- 5 Nov 2025 (estimated)
- Study completion
- 30 Nov 2025 (estimated)
- First posted
- 19 Sep 2024 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
A study aims to assess the most effective preventive interventions to address the widespread issue of dental caries, affecting an estimated 2 billion people in permanent teeth and over 500 million children in primary teeth globally. Notably, in Pakistan, over 90% of caries-affected teeth are untreated. Despite schools being a platform for public health initiatives, there is limited evidence on oral health promotion in low and middle-income countries. This study compares different preventive strategies' effectiveness and cost-efficiency for caries prevention in schoolchildren.
The randomized controlled trial will occur in Naval Schools of Karachi under the Pakistan Navy Educational Trust (PNET) over one year, including intervention and follow-up periods. The interventions include a combination of fluoride toothpaste, dietary counselling, and fissure sealant application. A multi-stage sampling method will select schools and classes, while convenience random sampling will select 180 children for the study. A single-blind trial will be conducted, with the data analyst unaware of the intervention groups.
Participants will be divided into three groups. Group 1 (Control) will use fluoride toothpaste and be instructed to brush twice daily. Group 2 (Intervention-1) will receive 14500 ppm fluoride toothpaste and oral health education. Group 3 (Intervention-2) will include the treatments from Group 2 plus fissure sealants on the first permanent molars. Parents in Groups 2 and 3 will receive a standardized advice sheet to reinforce oral hygiene practices at home.
The study will collect baseline demographic data, including age, gender, socioeconomic status, family education, existing oral hygiene practices, dental knowledge, and dentition status. Oral examinations will be conducted according to international standards. Statistical analysis will employ Chi-Square, ANOVA, and logistic regression tests, with a significance level set at 0.05.
The study aims to determine the most effective preventive strategy by comparing the reduction in dental caries incidence across the groups. The findings will guide recommendations for implementing the most effective intervention on a larger scale in schools, with the goal of reducing the burden of dental caries in children.
Detailed description
Ethical Approval approved by the BUHSC ethical committee. School administrations will be approached for permission. Consent forms will be sent to the parents of the children before the data collection visit. The data collection team comprised of 06 members will visit the selected schools. A signed consent form will be taken, and verbal consent will be obtained from the children as well. The children fulfilling the inclusion criteria will be sequenced as a list. Randomization will be done through SNOSE - a sequential number of opaque sealed envelopes will be done, and the students will then be allocated in 3 groups.
PI, Co-PI, and 05 team members will conduct oral examinations in the selected schoolyard or inside a classroom, following the standard international guidelines (WHO 2013). In addition, the baseline demographic data will also be collected comprising of age, gender, socioeconomic status (SES), family education and existing oral hygiene practices, dental knowledge, and dentition status by the parents and participants. Group 1 (Control) will be given fluoride toothpaste containing 1450 ppm Fluoride and will be asked to brush at least twice daily with a pea-sized amount of toothpaste, using the modified bass technique. This will be considered as control. Some intervention in the control group will also address the ethical issues. Parents will be guided for the tooth brushing.
Group 2 (Intervention -1) will be given fluoride toothpaste containing 1450 ppm Fluoride and will be asked to brush at least twice daily with a pea-sized amount of toothpaste and oral health education. A modified bass technique for tooth brushing will be used. Oral health education through audio-visual aids, pamphlets, and live demonstrations on study models will cover proper tooth brushing techniques, the use of a good toothbrush, and healthy eating habits, including special emphasis on proteins and dairy products and alternate use of sugars in daily routine. E.g. soft drinks that are high in sugar can be replaced with drinking milk and water.
Group 3 (Intervention -1) will be given fissure sealants on 1st permanent molar along with the strategy given to Group 2. Fissure sealing compounds, Glass ionomer will be used on school children who will qualify for inclusion criteria. Mobile Dental Unit and fissure sealant kit will be taken to the site and children will be provided fissure sealant in their setting.
In the intervention group (2 and 3) parents will also be given an Evidence-Based standardized parental advice sheet to reinforce instructions at home.
The saliva of school children will be collected by spitting in a test tube. For children over the age of 6, saliva can be collected using the expectoration, or spit method. In this process, the child is instructed to keep their mouth closed for three minutes without swallowing, allowing saliva to accumulate before spitting it into a collection tube. However, some children may struggle with this technique due to the challenge of not swallowing for an extended period. An alternative method is the drainage technique. Here, the child is first asked to swallow their saliva to stimulate the production of more saliva. Then, with their lips slightly parted, the saliva is allowed to drain directly into the collection tube The samples will be taken to the laboratory within 02 hours of collection Streptococcus mutans count will be conducted on collected saliva at the first visit to provide an initial bacterial count as baseline data before intervention and after six-month and 12-month bacterial count after the intervention. The primary medium used to identify streptococci is Mitis-Salivarius agar or its variant with bacitracin (MSB). Additionally, saliva's pH, flow rate, and buffering capacity will be measured in the lab. The first visit will be followed by six months and 12 months respectively. A preliminary pilot study will be undertaken with a limited sample size to assess the practicality of the interventions and enhance the process of collecting data.
The data collected through the questionnaire and log book filled by parents at home will be computerized, followed by converting it into the appropriate SPSS files. The outcome variables for assessing dental caries will be measured by ICDAS. The ICDAS is a two-digit coding method. One for caries and the other for sealant and restorations. In this research, only the caries coding method will be used. For caries, the method ranges from sound teeth (code 0), through enamel caries lesions (codes 1-3), to carious lesions in dentine (codes 4-6). For sealant and restoration, the method ranges from 0 to 8 as follows: 0 = Sound, 1 = Sealant, partial, 2 = Sealant, full, 3 = Tooth-coloured restoration, 4 = Amalgam restoration, 5 = Stainless steel crown, 6 = Porcelain or gold or Porcelain-Fused-to-Metal (PFM) crown or veneer, 7 = Lost or broken restoration, 8 = Temporary restoration (will not be used). Caries Codes (0 = sound tooth surface; A = first visual change in enamel; B = distinct visual change in enamel; 3 = enamel breakdown, no dentine visible; 4 = dentinal shadow (not cavitated into dentine); 5 = distinct cavity with visible dentine; 6 = extensive distinct cavity with visible dentine); Missing Teeth (97 = extracted due to caries; 98 = missing for other reasons; 99 = un-erupted).
Salivary indicators i.e. salivary flux - 0.3-0.4 ml/min. Salivary pH - 5-5.8, high acidity; 6.0-6.6, moderate acidity; 6.8-7.8, normal salivary pH Salivary buffer capacity - 3-30 mg/100 ml. Salivary Mutans count - < 10^5 CFU/ml saliva or ≥ 10^5 CFU/ml saliva. The study will use the CONSORT checklist for reporting the randomized control trial.
Study design
- Primary purpose
- Prevention
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 3
- Model description
- Control, Interventional group 1, Interventional group 2
| Arm | Type | Receives |
|---|---|---|
| tooth-brushing | Active comparator | Other: Tooth brushing, tooth paste containing 1450ppm fluorideIn Control arm, tooth brushing with fluoride toothpaste using pea-sized toothpaste, using bass technique. |
| tooth-brushing and dietary counselling | Active comparator | Other: Tooth brushing, tooth paste containing 1450ppm fluorideIn intervention arm 1, tooth brushing with fluoride toothpaste using pea-sized toothpaste, using the bass technique, and dietary counselling. |
| tooth-brushing , dietary counselling and fissure sealing of 1st permanent molar | Active comparator | Other: Tooth brushing, tooth paste containing 1450ppm fluorideIn the intervention arm 2, tooth brushing with fluoride toothpaste using pea-sized toothpaste, using the bass technique, dietary counseling, and application of fissure sealant on a permanent first molar. |
Who may qualify
- Ages
- 6 to 7 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child
Key inclusion criteria (1 listed)
- Schoolchildren aged 6-7 years Sound 1st permanent molars Consent obtained from parents/guardians Cooperative Children
Key exclusion criteria (1 listed)
- 1st Permanent molar has not erupted. Children with disability. Special Children (e.g. Down syndrome)
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Tooth brushing, tooth paste containing 1450ppm fluorideAlso: dietary counselling, fissure sealent, Glassionomer cementbrushing with fluoride toothpaste, dietary counselling for caries prevention and application of fissure sealant compound on first permanent t molars. | Other | tooth-brushing, tooth-brushing , dietary counselling and fissure sealing of 1st permanent molar, tooth-brushing and dietary counselling |
Primary outcome
Prevention of dental Caries
Time frame: 1 year
Compare the effectiveness of the combination of different preventive strategies which include tooth brushing with fluoride toothpaste, dietary counselling, and fissure sealant application for reducing the incidence of dental caries among school children
2 secondary outcomes
Dietary Analysis
Time frame: 1 year
Streptococcus mutans in Saliva
Time frame: 1 year
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Sep 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Kulsoom F Rizvi, MSc principal investigator
Bahria University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Tooth brushing, tooth paste containing 1450ppm fluoride in people with Prevention of Dental Caries, run by Bahria University at 1 site in Pakistan.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 23 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Prevention of dental Caries (time frame: 1 year). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Sep 2025.