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Effect of Three Types of Fluoride Varnish in Preventing Early Childhood Caries

The University of Hong Kong (HKU) logo

The University of Hong Kong (HKU)

Status

Unknown

Conditions

Early Childhood Caries

Treatments

Other: NaF-CPP-ACP
Other: NaF vanish
Other: NaF-TCP

Study type

Interventional

Funder types

Other

Identifiers

NCT04274569
GRF Project HKU17106318

Details and patient eligibility

About

This study evaluates and compares the effect of two types of calcium- and phosphate-containing fluoride varnishes to conventional fluoride varnishes in preventing early childhood caries.

Full description

Fluoride vanish is the most commonly used professionally applied topical agent. Traditional fluoride vanish application has been reported to exhibit significant caries inhibiting effect in both permanent teeth and primary teeth. The greatest advantage of fluoride vanish is its ability to adhere to tooth tissues for a longer period of time that enables improved fluoride uptake. It allows continuous release of fluoride ions into enamel, dentine, plaque, and saliva.The main action of topical fluoride is to retard demineralization and promote remineralization of enamel by the uptake of calcium and phosphates from saliva. The proposed mechanism of action of topical fluoride is the formation of intraoral calcium fluoride reservoirs, which are retained on enamel and slowly released to inhibit mineral loss during demineralization.

However, the formation of the intraoral calcium fluoride reservoirs is limited by the availability of intraoral calcium and fluoride ions. Low concentration of salivary calcium and phosphate ions leads to mineral deposition only at the surface of enamel as a result of low ion concentration gradient. Deposition of minerals at the surface of enamel alone may not improve the structural properties of the deep part of the incipient carious lesions. Hence, many manufacturers have modified fluoride vanish to include calcium and phosphate ions in an attempt to further improve efficacy of fluoride varnishes.

The in vitro remineralizing effects of calcium- and phosphate-containing fluoride vanishes are encouraging and scientifically sound, a longitudinal, high quality clinical study is needed to verify the laboratory findings.

Enrollment

570 estimated patients

Sex

All

Ages

3 to 4 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Generally healthy children age between 3-4 of age with unremarkable medical history and at high caries risk with at least one carious lesion (precavitated or cavitated) (Agouropoulos et al 2014). The high caries risk children are chosen because it is anticipated that they will benefit more from the topical fluoride varnish application than the low caries risk children.

Exclusion criteria

  • Patients who had received professional fluoride application in the past 6 months

    • Patients with underlying medical history or special health care needs
    • Patient who are uncooperative or refuse the treatment
    • Patient who are allergic to milk protein (as MI VarnishTM contains "casein, a milk protein)
    • Patient with contraindication for fluoride varnish e.g. hypersensitivity to colophony and/or any other constituents
    • Patient who have primary teeth with enamel hypoplasia

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

570 participants in 3 patient groups

Sodium fluoride (NaF)
Active Comparator group
Description:
Group 1: Quarterly application of a 5% NaF varnish (Duraphat® Varnish, Colgate-Palmolive Ltd, (UK) Ltd., Guildford, Surrey, UK)
Treatment:
Other: NaF vanish
NaF plus tricalcium phosphate (TCP )
Experimental group
Description:
Group 2: Quarterly application of 5% NaF-TCP (ClinproTM White Varnish; 3M ESPE, St Paul, MN, USA)
Treatment:
Other: NaF-TCP
NaF plus CPP-ACP
Experimental group
Description:
Group 3: Quarterly application of a 5% NaF plus casein phosphopeptide-stabilized amorphous calcium phosphate complexes (CPP-ACP) (MI Varnish TM; GC corporation, Itabashi-Ku, Tokyo, Japan)
Treatment:
Other: NaF-CPP-ACP

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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