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Effectiveness of Silver Diamine Fluoride in Arresting Dental Caries

Effectiveness of Silver Diamine Fluoride in Arresting Dental Caries in Deciduous Molars: a Controlled and Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03063307
Enrollment
119
Registered
2017-02-24
Start date
2016-09-20
Completion date
2020-12-31
Last updated
2021-03-04

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

Conditions

Dental Caries in Children

Keywords

Tooth, Deciduous, Dental Caries, Glass Ionomer Cements, Dental Atraumatic Restorative Treatment, Cariostatic Agents, Fluorides

Brief summary

The present study aims to evaluate, through a controlled clinical randomized study,the effectiveness of silver diamine fluoride in arresting dentin caries lesions in primary molars when compared to atraumatic restorative treatment.

Detailed description

The present controlled clinical randomized study aiming at evaluating the effectiveness of silver diamine fluoride (SDF) in arresting dentin caries lesions on the occlusal surface of primary molars when compared to atraumatic restorative treatment (ART). For this, 118 healthy children aged 2-5 years with at least one active dentin carious lesion, with no signs of pain or pulp involvement. The participants will be allocated randomly to one of two treatment groups: (1) Test Group - SDF and (2) Control Group - ART. The International Caries Detection and Assessment System (ICDAS) will be used to determine caries diagnosis and activity. In both groups, the guardians and children will receive oral hygiene instructions and will be advised about eating habits and fluoride dentifrice use.The clinical success will be verified through examinations performed by a blinded operator, after 3, 6 and 12 months, with clinical evaluations to detect caries arresting, representing the primary outcome of the study.

Interventions

OTHERSilver Diamine Fluoride

Sponsors

Rio de Janeiro State University
CollaboratorOTHER
Universidade Federal do Rio de Janeiro
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
2 Years to 5 Years
Healthy volunteers
Yes

Inclusion criteria

* CHILDREN * aged 2 to 5 years; * who are in good general health; * have at least one active dentin carious lesion on the occlusal surface of primary molars corresponding to ICDAS codes 5 or 6.

Exclusion criteria

* CHILDREN * with systemic or neurological diseases; * whose families intend to move from Rio de Janeiro next year; * with a history of allergy to silver or any substance present in the different materials to be used for treatment. TEETH * with spontaneous or provoked pain, dental mobility or radiographic signs of involvement or possible pulp involvement; * shows possible pulp involvement by radiographic examination

Design outcomes

Primary

MeasureTime frameDescription
Caries arrestingThe follow-up oral examinations will be conducted every 3 months for 48 months totallyThe main outcome of the study will be the observation of the proportion of arrested caries lesions in the test group, compared to the control group.

Secondary

MeasureTime frameDescription
Duration of the intervention visit1 yearTime (in minutes) spent on each type of intervention (DFP x ART)
Cost1 yearThe cost of each treatment will be recorded and compared to each other
Aesthetic perception and treatment satisfactionFirst appointment, 3,6 and 12 months after treatment.Information on aesthetic perception will be obtained through a questionnaire, addressed to parents / guardians.
AnxietyFrom allocation up to two weeks.A facial imaging scale will be used to assess the degree of anxiety of children 3 years of age or older. before and after first exam and treatment appointments.
Quality of life assessmentFirst appointment,15 days and 3 months after treatment.Information about quality of life will be obtained through the questionnaire Brazilian Early Childhood Oral Health Impact Scale (B-ECOHIS), addressed to parents / guardians.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026