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Dental Caries clinical trials

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NCT ID: NCT04562675 Completed - Caries,Dental Clinical Trials

Long-term Effects of a Lay Health Advisor Intervention on Immigrant Children's Caries

Start date: August 27, 2012
Phase: N/A
Study type: Interventional

The aim of this study was to evaluate the long-term effectiveness of a lay health advisor (LHA) intervention on immigrant children's caries and preventive behaviors.This randomized controlled trial included mother-child pairs in the intervention group (IG) and a brochure-only control group (CG), respectively. The IG received a four-week one-on-one session by an LHA on caries-related knowledge and brushing techniques. Baseline and follow-up surveys were used to collect the data in caries experience and maternal caries preventive behavior.

NCT ID: NCT04560478 Completed - White Spot Lesion Clinical Trials

Comparing Fluoride Varnish and Sealant to Prevent White Spots in Orthodontic Patients

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is o compare the efficacy of CPP-ACP MI Varnish and ProSeal sealant in preventing white spot lesion (WSL) formation in orthodontic patients.

NCT ID: NCT04550546 Completed - Dental Caries Clinical Trials

Effects of Nystatin Suspension Oral Application on Oral Microbial Community

Start date: May 15, 2021
Phase: Phase 1
Study type: Interventional

The purpose of this study is to examine the effect of a prescription mouth rinse (Nystatin),an FDA approved drug, on the different types of bacteria in the mouth. Results from this study may help understand the effect that Nystatin oral rinse has on certain types of oral bacteria, which may also cause tooth decay.

NCT ID: NCT04512482 Completed - Dental Caries Clinical Trials

Evaluation of Oral Plaque Removal Utilizing an Adjunct Enzyme Pre-rinse

Start date: June 14, 2018
Phase: Phase 2
Study type: Interventional

This study aims to investigate the impact of a bromelain pre-rinse adjunct on oral plaque removal in orthodontic subjects. The study's null hypothesis states that there is no statistically significant difference in visual plaque scores among orthodontic subjects with or without proteolytic enzyme rinse aid.

NCT ID: NCT04488380 Completed - Dental Caries Clinical Trials

Clinical Performance of Glass Ionomer Versus Resin Composite Restorations

Start date: October 12, 2015
Phase: N/A
Study type: Interventional

The aim of this randomised-controlled, single-blind, split-mouth, and single-centre clinical trial was to evaluate the 2-year clinical performances of a high-viscosity glass ionomer and nanohybrid composite resin in occlusal restorations on mandibular second molar teeth in patients at risk for salivary contamination.

NCT ID: NCT04439877 Completed - Peri-Implantitis Clinical Trials

Exploring the Relationship Among Dental Caries, Nutritional Habits and Peri-implantitis

Start date: February 1, 2018
Phase:
Study type: Observational

Aim: A study was made of the prevalence, co-occurrence and association among caries, nutritional habits and peri-implant disease, with an analysis of the influence of other patient and implant factors upon peri-implant disease. Material and methods: The included subjects underwent a clinical examination and were asked to complete a questionnaire. Demographic data and potential lifestyle/behavioral variables were collected. Clinical and radiographic assessment allowed calculation of the decayed, missing and filled teeth (DMFT) index and peri-implant diagnosis. Uni- and multivariate logistic regression analyses were applied to identify predictors of peri-implant disease.

NCT ID: NCT04436913 Completed - Dental Caries Clinical Trials

Evaluation of Preventive Regimens With Different Toothpastes vs Fluoride Varnish & Toothpaste in High Caries Patients

Start date: January 16, 2021
Phase: N/A
Study type: Interventional

This study will be conducted in order to determine the prevention effect of caries preventive regimen using herbal toothpaste and regimen using fluoride toothpaste versus fluoride toothpaste and fluoride varnish on the caries risk of patients with high caries risk.

NCT ID: NCT04399369 Completed - Dental Caries Clinical Trials

Preventing Caries With Silver Diamine Fluoride

Start date: September 16, 2020
Phase: Phase 2
Study type: Interventional

Background: Early childhood caries (tooth decay, ECC) affected 55% 5-year-old Hong Kong children, and 70% of these children had gross destruction of the upper anterior teeth with negative long-term impacts on health and quality of life. The existing standard of care for prevention of ECC, topical application of 5% sodium fluoride (NaF) varnish, is inadequate. In Hong Kong and other parts of the world, 38% silver diamine fluoride (SDF) solution, applied topically to cavities, is used to arrest ECC. Work published by our research group suggests it likely also has a preventive effect of ECC. Moreover, SDF has been shown to be preventive in tooth decay in permanent teeth. Nevertheless, no pivotal clinical trial has been performed to support a change in usual practice. Aim: This is a Phase II single-centre randomized, double-blind, active-controlled, parallel-group pragmatic trial with two arms to assess the effectiveness of 38% SDF and 5% NaF in preventing new caries lesions in primary anterior teeth. Methods: 688 three-year-old kindergarten children who are healthy will be recruited, stratified by school, and block randomized to receive either 38% SDF (treatment group) or 5% NaF (standard treatment group) therapy on primary upper anterior teeth. This sample size is sufficient for a superiority trial with power at 90%, allowing for a 15% dropout rate. The primary outcome is the number of sound tooth surfaces that become cavitated caries per child at 12-month follow-up. The secondary outcome is the number of carious tooth surfaces developed after baseline that become arrested at 12-month for each child. Dental examinations for the status of caries (active or arrested) will be conducted by the same calibrated examiner. The examiner, children and children's parents will be blind to treatment allocation. Parents will be surveyed to study the children's oral health-related behaviours and socioeconomic backgrounds, which will allow the adjustment for effect modification. Possible results and implications: If the results are as anticipated, it will help change the standard of care for caries prevention. If adopted in Hong Kong, SDF therapy will prevent 20,800 (13% of the 160,000) kindergarten children from having caries developed in their anterior teeth, thus reduce significantly the burden of ECC of the children and related stress of their family. Moreover, the results will be widely available and increase adoption of SDF in other countries to reduce the global burden of ECC among children.

NCT ID: NCT04390256 Completed - Dental Caries Clinical Trials

Remineralization of Early Carious Lesion Using Natural Agents Versus Bioadhesive Polymers

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

This study will be conducted to evaluate: 1. The remineralization potential of natural agents (egg shell powder and clove extract) versus bioadhesive polymers (carbopol and carboxymethyl cellulose) with or without PH cycling using microhardness test. 2. The clinical efficacy of all agents in patients with early carious lesions.