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Dental Caries clinical trials

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NCT ID: NCT03785730 Suspended - Dental Caries Clinical Trials

Non-restorative Cavity Control in Anterior Cavitated Caries Lesion of Primary Teeth

CEPECO2
Start date: April 30, 2019
Phase: N/A
Study type: Interventional

Background: Studies have questioned the necessity of restoring cavitated carious lesion on primary teeth, once the control of biofilm is the most important factor to arrest these lesions. This randomized clinical trial aimed to compare the survival of teeth treated with a non-restorative cavity control (NRCC) compared to resin composite restorations (RCR) on proximal carious lesion in anterior primary teeth, as well as the impact of these treatments on patient-centered outcomes. Methods: A randomized clinical trial with two parallels arms (1:1) will be conducted. Children between 3 and 6 years old will be selected from the Center of Clinic Research of Pediatric Dentistry of Ibirapuera University (UNIB), a dental trailer (FOUSP) located on Educational Complex Professor Carlos Osmarinho de Lima, the Pediatric Dentistry Clinic of Santa Cecília University and from the Pediatric Dentistry Clinic of University Center UNINOVAFAPI. One hundred and forty-eight teeth will be randomly distributed in two experimental groups: (1) Selective removal of carious tissue and RCR; or (2) NRCC through cavity enlargement using metallic sandpaper. The primary outcome will be tooth survival after 6, 12, 18, and 24 months. The duration and the cost of dental treatments will be considered for the estimation of the cost-effectiveness of the evaluated treatments. The discomfort reported by the participants will be measured after each treatment using the FIS scale. The participants' satisfaction and perception of the parents/legal guardians will be evaluated through questionnaires. For the primary outcome, Kaplan-Meier's survival and Long-Rank test will be used for comparison between the two groups. All the variables will be modeled by Cox regression with shared fragility. Significance will be considered at 5%.

NCT ID: NCT03780270 Completed - Tooth Decay Clinical Trials

Preventive Treatment Approach of Early Caries Lesions With Contemporary Methods of Remineralization

Start date: June 16, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate 1. the additional therapeutic benefit of Curodont Repair for the treatment early occlusal carious lesions on permanent teeth in children compared fluoride varnish alone 2. the tooth gel Curodont Protect when using it after Curodont Repair instead of fluoride varnish

NCT ID: NCT03779893 Not yet recruiting - Caries, Dental Clinical Trials

Clinical Evaluation of Bioactive Resin Sealants vs Conventional Sealants in Permanent Molars

Start date: January 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This study will be conducted to evaluate the performance; in terms of retention and caries inhibition; of the newly introduced bioactive resin based pits and fissure sealant versus conventional resin based pits and fissure sealant in caries susceptible fissures in posterior molars in patients at risk of caries. Evaluation will be done by visual tactile examination & VistaCAM.

NCT ID: NCT03779698 Completed - Dental Caries Clinical Trials

BiodentineTM Versus Formocresol Pulpotomy Technique in Primary Molars

Start date: May 2014
Phase: Phase 4
Study type: Interventional

The objective of this clinical study was to prospectively compare the clinical and radiographic success rates of BiodentineTM pulpotomies versus formocresol pulpotomies in children vital primary molars. A randomized, split-mouth study design was used with a sample of 37 healthy children aged 4- to 8-year-old. A total of 56 pairs (112 teeth) of carious primary teeth, 1 pair per child, were selected for treatment. One tooth from each pair was randomly assigned to either the BiodentineTM pulpotomy group or the formocresol pulpotomy group. Children were followed-up at 3, 6 and 12 months for clinical evaluation and at 6 and 12 months for radiographic evaluation. Data were collected, tabulated and analyzed using Fisher exact and McNemar tests. The level of significance was set at P < 0.05.

NCT ID: NCT03770871 Completed - Dental Caries Clinical Trials

Indirect Pulp Treatment in Primary Molars

RCT
Start date: August 2016
Phase: Phase 4
Study type: Interventional

This study was conducted to evaluate the clinical and the radiographic success of Dycal and Vitrebond as indirect pulp treatment materials in primary molars.

NCT ID: NCT03770286 Completed - Dental Caries Clinical Trials

Treatment of Interproximal Cavities on Primary Molar Teeth With Silver Diamine Fluoride

Start date: January 22, 2019
Phase: Phase 3
Study type: Interventional

This study investigates whether 1) Silver diamine fluoride (SDF) application using Super Floss can arrest and/or reverse initial interproximal caries on primary molars and 2) whether SDF applied with Super Floss is more effective in arresting or remineralizing initial interproximal lesion in comparison to SDF applied without Super Floss or fluoride varnish applied alone.

NCT ID: NCT03764059 Completed - Clinical trials for Dental Caries Class II

Clinical Study of Filtek™ Bulk Fill Posterior Restorative in Class I and II Restorations

Start date: October 17, 2017
Phase: N/A
Study type: Interventional

Purpose of the Study:This study was to evaluate the 1 week, 1 year safety and effectiveness of dental composite resin (Filtek™ Bulk Fill Posterior Restorative) in restoring Class I and II dental cavities in posterior teeth.

NCT ID: NCT03763578 Completed - Dental Caries Clinical Trials

Dental Caries Prevention by a Natural Product

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The objective is to conduct an RCT to evaluate the effectiveness of Licorice in comparison to standard caries preventive measures for the prevention of new carious lesions in high caries risk patients.

NCT ID: NCT03761485 Completed - Caries, Dental Clinical Trials

Dental Fluorosis Risk by the Use of Acidulated Fluoride Dentifrice

Start date: January 15, 2015
Phase: Phase 4
Study type: Interventional

This research aimed to evaluate the risk of dental fluorosis by using an experimental fluoridated acidulated dentifrice compared to conventional dentifrices in two-to-four-year-old children residing in a non fluoridated area by the concentration of fluoride incorporated in childrens' nails, as well as the incorporation of F into the biofilm. Two hundred and ten children participated on this study. They were randomly allocated into three groups differing according to the type of dentifrice used over 12 months: G1:1100 ppm F, pH 4.5; G2:750 ppm F, pH 4.5; G3:1100 ppm F, pH 7.0. The dentifrice was placed on the toothbrush using the "drop" technique. The toenails of the biggest toe were collected in three moments, corresponding to the experimental period of use of the dentifrices (T1, T2 and T3), as well as the biofilm which was collected twice, 5 and 60 minutes after brushing. The nails and biofilm fluoride concentration were analyzed on a specific electrode using the HMDS diffusion facilitated technique.

NCT ID: NCT03753256 Recruiting - Dental Caries Clinical Trials

Evaluation of Optical Coherence Tomography in Dentistry

Start date: December 4, 2017
Phase: N/A
Study type: Interventional

Optical coherence tomography (OCT) is a medical diagnostic tool, providing non-invasive, non-radiative and high resolution imaging. OCT has been established since many years in ophthalmology. In dentistry the diagnostic potential of OCT is currently increasingly being noticed. This clinical study includes two individual trials: (i) Longitudinal assessment of surface sealant thickness using optical coherence tomography and (ii) comparison of crevicular fluid levels of inflammatory cytokines after the application of surface sealants.