Clinical Analysis of a Risk-graded and Comprehensive Intervention for Early-childhood-caries

Early Childhood Caries Clinical Trial

Official title:

Clinical Analysis of Cariogram and Cariostat for Risk Assessment and Comprehensive Intervention of Early-childhood-caries

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05260216
• Other study ID #: CARGACIFECC
• Status: Recruiting
• Phase: N/A
• Start date: November 4, 2021
• Est. completion date: August 31, 2024

Study information

• Verified date: December 2021
• Source: Beijing Friendship Hospital
• Contact: Menglin Cheng, Doctor
• Phone: 80838416
• Email: chengmenglin2011[@]126.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Cariogram and Cariostat will be used to assess the risk of caries in kindergarten children aged 3 years. Routine preventive measures will be taken for children at low risk of caries, and intensive intervention measures will be taken for children at medium and high risk. Routine measures will be taken for the control group. After one and two year, the prevalence of caries in the experimental group and the control group should be evaluated, and the cost-effectiveness evaluation will be conducted.

Description:

Caries risk-graded intervention for preschool children is needed as different child has different risk to suffer from caries.

Cariogram and Cariostat are two different and common caries risk assessment tools. Cariogram is a complicated but economical computer program which is more sensitive for caries risk assessment. Cariostat is a biological reagents with high specificity but it may be expensive to use for large numbers of children.

The experimental group will be divided into two subgroups, one use Cariogram and the other use Cariostat to assess the risk. Based on the results of the assessment, children with low risk of caries will get routine prevention including twice fluorinated foams each year and hygiene. Children with middle or high risk of caries will receive twice fluorinated varnish each year and professional caries treatment in addition to routine prevention.Routine prevention will be taken for the control group with both Cariogram and Cariostat assessment.

Follow-up will arrange one and two years after baseline recruitment. All participants will receive oral health-related questionnaires at baseline and follow-up.

The prevalence of caries in the experimental group and the control group should be evaluated, and the cost-effectiveness evaluation will be conducted.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 480
• Est. completion date: August 31, 2024
• Est. primary completion date: August 31, 2022
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 3 Years to 4 Years

Eligibility

Inclusion Criteria:

1. Junior kindergarten children who enter the kindergarten in September 2021 and can cooperate with the oral health examination.

2. Parents of children fully understand the purpose of the study, cooperate with the questionnaire survey during the study, give informed consent and sign the informed consent form.

3. The child has no serious systemic diseases, has not taken hormones and immunosuppressants within 6 months, and has no history of antibiotic use within 1 month,and is not allergic to fluoride.

Exclusion Criteria:

1. Parents of children refuse to provide information about children's oral health or questionnaires.

2. Children cannot cooperate with oral health examination.

3. The child has a serious systemic disease that may affect the results of the study.

4. Children who are allergic to fluoride.

Related Conditions & MeSH terms

• Early Childhood Caries

Intervention

Combination Product:
• Comprehensive prevention and treatment
Children with low risk of caries will receive routine prevention including fluoride foam application twice a year and oral hygiene guidance. Children with middle or high risk of caries will receive fluoride varnish application twice a year and caries restorative treatment in addition to routine prevention. The risk-graded intervention is one kind of comprehensive prevention and treatment.
• Routine prevention
Routine prevention includes fluoride foam application twice a year and oral hygiene guidance.

Locations

Country	Name	City	State
China	Beijing Friendship Hospital, Capital Medical University	Beijing	Beijing

Sponsors (1)

Lead Sponsor	Collaborator
Beijing Friendship Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Decay teeth,Missed teeth and filled teeth (DMFT) and the change between different time points.	The average value of the sum of the number of decayed teeth, the number of filled teeth, and the number of missed teeth due to caries.	Baseline, one year follow up and two year follow up.
Secondary	Caries prevalence and the change between different time points.	The proportion of population with caries in the whole participants.	Baseline, one year follow up and two year follow up.