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N/A N=84 Randomized Treatment

A Clinical Trial of Silver Diamine Fluoride to Arrest Early Childhood Caries in Young Children

Early Childhood Caries

Enrolled (actual)
84
Serious AEs
0.0%
Results posted
Sep 2023
Primary outcome: Primary: Overall Arrest Rates — 81.3; 61.5; 78.1; 95.8 percentage of lesions arrested

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Silver diamine fluoride (Device)
Age
Pediatric
Sex
All
Sponsor
University of Manitoba
Primary completion
Mar 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Arrest Rates
81.3; 61.5; 78.1; 95.8; 72.0; 98.0
PRIMARY
Anterior Teeth Arrest Rates
83.0; 75.3; 85.0; 97.9; 74.0; 99.2
PRIMARY
Posterior Arrest Rates
79.2; 48.6; 63.5; 93.1; 70.0; 95.2

Summary

Silver diamine fluoride (SDF) is an antibiotic liquid that has the potential to arrest Early Childhood Caries in young children and delay treatment until children can be seen in outpatient settings. While SDF received approval for clinical use in Canada in 2017 (i.e. Advantage Arrest TM/38% SDF), there has been little guidance on the frequency and duration of applications. This study evaluates the use of SDF at different frequencies to manage dental caries in young children. Potential oral microbiome changes in children receiving SDF treatments are also studied. The investigators hypothesize that two applications of SDF at different frequencies will yield similar arrest rates, and that SDF negatively influences the population of cariogenic bacteria in the oral microbiome. The investigators propose a randomized clinical trial to study the use of SDF to arrest cavitated lesions in primary teeth at different application regimens. Regimen 1 will be two applications of SDF four months apart. Regimen 2 will be two applications of SDF six months apart. Regimen 3 will be two applications of SDF one month apart. Arrest of caries lesions will be determined by assessing clinical hardness, colour change and size of lesions at baseline, at second visit, and at the final study visit. Children < 72 months of age with active caries will be recruited from community-based dental clinics or who are currently on a wait list for dental surgery under general anesthesia in Winnipeg, Manitoba. SDF will be applied on the day of recruitment to cavitated lesions involving dentin followed by 5%NaFV. Depending on which frequency regimen children are randomized to, participants will return for a second visit. At the second visit, caries lesions treated with SDF at baseline will be assessed to see if caries is arrested. A second application of SDF will be applied to these initially treated caries lesions followed by 5%NaFV. Participants will return for a third and final study visit according to the schedule of their randomized grouping. Caries lesions previously treated by SDF will be assessed once again. To investigate SDF's influence on the human oral microbiome, children from each regimen will have plaque samples collected. Samples will be obtained prior to SDF application at baseline, at the first follow-up visit, and at the final visit. Following nucleic acid isolation from plaque samples and amplicon sequencing, data analysis will be performed in lab using established methods.

Eligibility Criteria

Inclusion Criteria

  • Child is < 72 months of age with early childhood caries (ECC) with active lesions (International Caries Detection and Assessment System codes 5 or 6).
  • Child has ≥ 1 primary tooth with caries that is eligible to receive SDF. Eligible primary teeth must: a) have soft cavitated caries lesions extending into dentin; b) the cavitated lesions must allow for direct application of silver diamine fluoride (SDF). Teeth that meet any of the PUFA (pulpal involvement, ulceration, fistula, and abscess) index criteria (i.e. spontaneous pain due to caries, pulp exposure, mobility, signs of pulpal infection such as abscess, fistula, or swelling) will be excluded. However, a child would still be eligible even if they have at least one tooth that meets PUFA criteria, but other eligible teeth with caries do not.

Exclusion Criteria

  • Child is allergic or has a sensitivity to silver or other heavy metal ions.
  • Child has hereditary generalized developmental defects of enamel (e.g. Amelogenesis Imperfecta, Dentinogenesis Imperfecta)
  • Child has severe medical problems that limit participation.
  • Child requires immediate rehabilitation under general anesthesia (GA) because of severe infection or pain.
  • Antibiotic use within the last 2 weeks.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04054635). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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