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Caries Cognition and Identification in Adults

Caries Associated With Restorations or Sialants Cognition and Identification in Adults

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03108586
Acronym
CaCIA
Enrollment
185
Registered
2017-04-11
Start date
2016-09-01
Completion date
2032-12-01
Last updated
2023-04-26

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

Conditions

Secondary Caries

Keywords

restorations, diagnosis, secondary caries, treatment decision

Brief summary

This study will evaluate the effect of the International Dental Federation (FDI) criteria, compared to CARS (Caries Associated with Restorations or Sealants) detection criteria for evaluation of caries lesions around restorations in permanent teeth, in the outcomes related to oral health of adults, in a randomized clinical trial.

Detailed description

The study will consist of a randomised controlled trial of two parallel groups. One group will correspond to adults who will receive the diagnosis and indication of treatment according to the standard criteria, following the FDI criteria to classify the restorations marginal conditions and the presence of secondary caries (traditional group). And the other group will receive a diagnosis and treatment decision according to a minimal intervention approach, using as reference the detection criteria Caries Associated with Restorations or Sealants (CARS) - ICCMS (International Caries Classification and Management System) - conservative group). Patient evaluations will be performed yearly after 12 months. The primary outcome will be the number of surfaces restored with the need for new interventions. Secondary outcomes will be the impact of oral health on quality of life and cost-effectiveness.

Interventions

Dental treatment of all dental needs present in adults related or not to the dental caries

Sponsors

Federal University of Pelotas
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Masking description

Patients, clinical operators responsible for dental treatment, and the examiner who will assess the outcomes will be blind to the allocation group of the participants.

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Patients seeking dental treatment at the School of Dentistry; * Age between 18 and 60 years; * Patients who present at least one restoration of composite resin or amalgam to posterior and/or anterior teeth.

Exclusion criteria

* Patients who refuse to participate in the research; * Patients included in other surveys that involve restorations or are in systematic attendance at another clinic or service; * Patients who present systemic conditions or chronic diseases that require differentiated care and follow-up - these will be referred to the specific services available at the Faculty of Dentistry; * Patients who reside in other locations and who can not return for periodic follow-up of the interventions.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in number of surfaces restored requiring new intervention12 months, 24 monthsThe primary endpoint will be the number of surfaces restored requiring intervention, which is composed of the sum of components with different levels of severity: number of surfaces with new caries lesions, number of surfaces restored in need of repair, replacement, teeth with episodes of pain, teeth requiring endodontic treatment or extraction.

Secondary

MeasureTime frameDescription
Cost-effectiveness measured by a scale12 months, 24 monthsEffectiveness will be measured through the number of restored surfaces without intervention. The cost-effectiveness ratio will be expressed by the cost ratio of the FDI and CARS criteria and effectiveness (number of surfaces without the need for new interventions)
Impact of intervention on quality of life measured by a validated questionnaire - OHIP-14 (Oral Health Impact Profile-14)12 months, 24 months

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026