Clinical Trials Directory

Trials / Completed

CompletedNCT04124887

Remineralization Effect of Fluoride Varnishes on Permanent Molars

Remineralization Effect of NaF, NaF With TCP, NaF With CPP-ACP, and NaF With CXP Varnishes on Newly Erupted First Permanent Molars: a Randomised Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Kırıkkale University · Academic / Other
Sex
All
Age
6 Years – 7 Years
Healthy volunteers
Accepted

Summary

The aim of this study was to evaluate and compare the efficacy of NaF, NaF with TCP, NaF with CPP-ACP, and NaF with CXP varnishes on newly erupted first permanent molar teeth. The study was carried out in 40 healthy, high caries risk children (DMFS \>8), aged six to seven years with newly erupted permanent first molars who referred to the Pediatric Dentistry Clinic of Kırıkkale University Faculty of Dentistry, Kırıkkale, Turkey. A total of 140 teeth were divided randomly into four groups and the varnishes were applied to the determined teeth at baseline, one and three months. The same varnish was used, if there is more than one first molar to be applied of the same patient. The groups were comprised as follows: Group 1: Duraphat Varnish containing 5% NaF (Colgate-Palmolive, NSW, Australia) (n = 35), Group 2: Clinpro™ White Varnish containing 5% NaF with TCP (3M ESPE, MN, USA) (n = 35), Group 3: Embrace ™ Varnish containing 5% NaF with CXP (Pulpdent, MA, USA) (n = 35), Group 4: MI Varnish containing 5% NaF with CPP-ACP (GC, Tokyo, Japan) (n = 35). All dental treatments of the patients were completed before the varnish application and oral hygiene instructions were given to all children at the start of the study. Patients were called for follow up appointments at 1, 3 and 6 months, and in the follow-up period DIAGNOdent device (laser fluorescence scanning) was used to monitor mineralization changes. LF measurements were made at baseline (T0), after one month (T1) three months (T2) and six months (T3). Within and between group comparisons were analysed statistically.

Conditions

Interventions

TypeNameDescription
DRUGSodium FluorideSodium Fluoride varnish was applied to the targeted teeth at baseline, one and three months.
DRUGTricalcium PhosphateVarnish with Tricalcium Phosphate was applied to the targeted teeth at baseline, one and three months.
DRUGXylitol-coated calcium and phosphateVarnish with Xylitol-coated calcium and phosphate was applied to the targeted teeth at baseline, one and three months.
DRUGCasein phosphopeptide amorphous calcium phosphateVarnish with Casein phosphopeptide amorphous calcium phosphate was applied to the targeted teeth at baseline, one and three months.

Timeline

Start date
2017-02-03
Primary completion
2018-02-08
Completion
2018-02-15
First posted
2019-10-14
Last updated
2019-10-15

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04124887. Inclusion in this directory is not an endorsement.