Skip to content

CARDEC-PEL: Comparison of Two Methods of Caries Risk Assessment in Children

CARies DEtection in Children-Pelotas (CARDEC-PEL): Comparison of Two Methods of Caries Risk Assessment in Children

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03969628
Enrollment
250
Registered
2019-05-31
Start date
2019-06-01
Completion date
2028-06-01
Last updated
2023-04-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Caries,Dental

Brief summary

The aim of the study was to compare dental caries treatment and follow-up based on an elaborate and individualized assessment of caries risk in children, to a simpler risk assessment strategy by means of a double-blind randomized clinical trial of two years monitoring. Participants will be children from 7 to 11 years old, who pass through the screening of the Children's Clinic of the Faculty of Dentistry of the Federal University of Pelotas and fulfill the inclusion criteria. A randomized, stratified sample of approximately 250 children will be included in the study, one group will be composed of children undergoing dental caries-related treatment and maintenance, guided by an individualized and multivariate risk assessment, and another group of children treated based on dental caries experience alone in the deciduous and / or permanent dentition. Recruitment will begin at the beginning of 2019, and participants will be followed up for 24 months. Parents will respond to an anamnesis, 24-hour dietary recall, food frequency questionnaire, and oral and general health-related quality of life questionnaire, children will undergo a clinical examination to assess caries, according to the International Caries Detection and Assessment System (ICDAS) in its simplified form and evaluation of caries activity. Dental treatments and return intervals will be designated according to the individual risk of the patient detected in the initial approach according to the group. The study evaluations consist of baseline, 12 months and 24 months, data will be transferred to spreadsheets after the different phases of the study. Primary outcomes (number of dental surfaces requiring operative intervention) and secondary outcomes will be analyzed by Student's t test, quality of life and quality of life related to oral health, will be assessed at the beginning of the study and at the end of treatment, and compared between the groups.

Interventions

DIAGNOSTIC_TESTICCMS

Risk caries assessment will consider ICCMS criteria

Sponsors

Federal University of Pelotas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 11 Years
Healthy volunteers
Yes

Inclusion criteria

* Individuals aged 7 years months to 11 years; * Children seeking dental treatment at the Pediatric dentistry university clinic in Pelotas (UFPel)

Exclusion criteria

* Medical and/or behavioral conditions that requires special considerations regarding management/treatment of the child

Design outcomes

Primary

MeasureTime frameDescription
New caries lesionsfrom baseline (first measurement) to 24monthsIncremental number of dental surfaces with operative treatment needs. This outcome will be assessed by the new caries lesions and / or progression of lesions previously diagnosed / treated and number of treated surfaces which will need restoration replacement, endodontic treatment or extraction after the treatment plan.

Secondary

MeasureTime frameDescription
Quality of life scorefrom baseline (first measurement) to 24monthsImpact on oral health related quality of life measured by a validated questionnaire (CPQ)

Countries

Brazil

Contacts

Primary ContactMarina S Azevedo, PhD
marinasazevedo@gmail.com555332602830

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026