Preventing Early Childhood Caries With Silver Diamine Fluoride
Primary Purpose
Dental Caries
Status
Recruiting
Phase
Phase 2
Locations
Hong Kong
Study Type
Interventional
Intervention
silver diamine fluoride
sodium fluoride
Sponsored by
About this trial
This is an interventional prevention trial for Dental Caries
Eligibility Criteria
Inclusion Criteria:
- generally healthy, with parental consents
Exclusion Criteria:
- uncooperative and difficult to manage, have major systemic diseases such as porphyria, or are on long-term medication such as anti-epileptic drugs.
Sites / Locations
- Local kindergartensRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
silver diamine fluoride
sodium fluoride
Arm Description
38% silver diamine fluoride
5% sodium fluoride
Outcomes
Primary Outcome Measures
caries prevention
the number of sound tooth surfaces that become cavitated caries per child
Secondary Outcome Measures
Full Information
NCT ID
NCT04075474
First Posted
August 28, 2019
Last Updated
December 8, 2022
Sponsor
The University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT04075474
Brief Title
Preventing Early Childhood Caries With Silver Diamine Fluoride
Official Title
Preventing Early Childhood Caries With Silver Diamine Fluoride - a Randomised Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
December 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 27, 2020 (Actual)
Primary Completion Date
June 30, 2023 (Anticipated)
Study Completion Date
June 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The University of Hong Kong
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
Background: Silver diamine fluoride (SDF) solution is effective in arresting early childhood caries (ECC). Previous studies suggested that it might exert a preventive effect in managing ECC. However, no well-designed clinical trial has been performed to study this topic. The aim of this randomised clinical trial is to assess whether 38% SDF is superior to 5% sodium fluoride (NaF) varnish in preventing new carious lesions in primary anterior teeth.
Methods/Design: This is a Phase II single-centre randomized, double-blind, active-controlled, parallel-group pragmatic trial. The hypothesis tested is that 38% SDF is more effective than 5% NaF in preventing new caries development in primary anterior teeth. Approximately 2,100 three-year-old kindergarten children who are generally healthy and with parental consent will be recruited. This sample size is sufficient for an appropriate statistical analysis of superiority trial with power at 80%, allowing for a 15% drop-out rate. Stratified randomization will be adopted for the intervention allocation. The intervention is either 38% SDF or 5% NaF (as positive control) therapy on primary upper anterior teeth. Dental examination followed by fluoride therapy will be conducted every six months until 30 months in kindergartens by a single examiner. The examiner, children and children's parents will be blinded to the treatment allocation. Questionnaire survey will be conducted to study the children's oral health-related behaviours and their socioeconomic backgrounds.
Discussion: The effectiveness of 38% SDF in preventing ECC remains uncertain. If the results are as anticipated, it will help change the standard of care that using 5% NaF for ECC prevention. In addition, the results will be widely available and increase adoption of SDF in other countries to reduce the global burden of ECC.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dental Caries
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
730 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
silver diamine fluoride
Arm Type
Experimental
Arm Description
38% silver diamine fluoride
Arm Title
sodium fluoride
Arm Type
Active Comparator
Arm Description
5% sodium fluoride
Intervention Type
Device
Intervention Name(s)
silver diamine fluoride
Intervention Description
38% SDF on primary upper anterior teeth
Intervention Type
Device
Intervention Name(s)
sodium fluoride
Intervention Description
5% NaF on primary upper anterior teeth
Primary Outcome Measure Information:
Title
caries prevention
Description
the number of sound tooth surfaces that become cavitated caries per child
Time Frame
at 30-month follow-up
10. Eligibility
Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
4 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
generally healthy, with parental consents
Exclusion Criteria:
uncooperative and difficult to manage, have major systemic diseases such as porphyria, or are on long-term medication such as anti-epileptic drugs.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Chun Hung Chu, PhD
Phone
(+852)28590287
Email
chchu@hku.hk
Facility Information:
Facility Name
Local kindergartens
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32019596
Citation
Gao SS, Chen KJ, Duangthip D, Wong MCM, Lo ECM, Chu CH. Preventing early childhood caries with silver diamine fluoride: study protocol for a randomised clinical trial. Trials. 2020 Feb 4;21(1):140. doi: 10.1186/s13063-020-4088-7.
Results Reference
derived
Learn more about this trial
Preventing Early Childhood Caries With Silver Diamine Fluoride
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