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Dental Caries clinical trials

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NCT ID: NCT02044081 Completed - Dental Caries Clinical Trials

Phase 2, Safety & Microbiology Study of C16G2 in Multiple Oral Gel &/or Mouth Rinse Doses to Healthy Adults

Start date: February 2014
Phase: Phase 2
Study type: Interventional

The focus of the study is to evaluate the safety of multiple study drug administrations and the study drug selectively reducing or eliminating a specific bacteria in the mouth. It will compare a liquid and gel product applied in different modes.

NCT ID: NCT02036151 Completed - Clinical trials for Dental Caries and Streptococcus Mutans Count

Impact of Maternal Xylitol Consumption on Mutans Sterptococci

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The study was designed to determine whether maternal xylitol consumption through regular chewing of xylitol gums can affect the salivary mutans streptococci (MS), dental caries, and dental plaque levels of their children.

NCT ID: NCT02027922 Completed - Caries Clinical Trials

Clinical Effectiveness of Various Professionally Applied Fluoride Prophylaxes in Groups at High Risk

Start date: November 2013
Phase: N/A
Study type: Interventional

The study is to compare the prophylactic and therapeutic clinical effectiveness of two fluoride varnishes in children at high caries risk. It was hypothesized, the use of Fluor Protector S (I) fluoride varnish in children with deciduous teeth at high risk of caries (P) reduces caries and the activity/remineralisation of carious enamel spots (transformation of White Spot Lesion into D (decay)) (O), similarly to what occurs after the use of Duraphat varnish (C).

NCT ID: NCT02020681 Completed - Dental Caries Clinical Trials

Effect of Curodont Repair or Placebo on the Remineralisation in Patients With Class 5 Carious Lesions

Start date: September 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the therapeutic benefit of Curodont Repair for the treatment of early buccal carious lesions compared to placebo.

NCT ID: NCT02019563 Completed - Dental Caries Clinical Trials

MTA/FS Pulpotomy for Vital Primary Incisors: A Randomized Controlled Trial

MTA/FS
Start date: September 2010
Phase: Phase 2
Study type: Interventional

To compare radiographic and clinical outcomes and survival of mineral trioxide aggregate/ferric sulfate (MTA/FS) pulpotomy and root canal therapy (RCT) in carious vital primary maxillary incisors.

NCT ID: NCT02018822 Completed - Dental Caries Clinical Trials

Evaluate the Effectiveness of an Experimental Urethane Dimethacrylate Resin Based Dental Composite Material

Start date: June 2013
Phase: N/A
Study type: Interventional

This double blind randomized controlled prospective clinical trial will compare the clinical success of two tooth colored resin composite dental filling materials - TPH3 (Dentsply Caulk) and an experimental urethane dimethacrylate resin based composite resin (Dentsply Caulk) for wear resistance, staining and marginal seal using modified Ryge criteria to evaluate the posterior restorations for 24 months in duration

NCT ID: NCT02017886 Completed - Periodontitis Clinical Trials

Salivary IgA and Cytokines Response to Dietary Supplementation of Lactobacillus Reuteri

Start date: November 2013
Phase: N/A
Study type: Interventional

To evaluate the effect of daily ingestion of the probiotic Lactobacillus reuteri on the levels of secretory IgA and the cytokines Il1-beta, IL-6, IL-8 and IL-10 in saliva of healthy young adults.

NCT ID: NCT02003820 Completed - Clinical trials for Autism Spectrum Disorder

Using Video Modeled Social Stories to Improve Oral Hygiene in Children With Autism Spectrum Disorder

Start date: July 2014
Phase: N/A
Study type: Interventional

We hypothesize that oral hygiene habits in children 8-12 years of age can be improved using video format Social Story intervention techniques. The purpose of this study is to investigate the effectiveness of video format social stories used to inform and educate children and parents about proper dental hygiene technique over a 6 week intervention period. We will measure the success of intervention using data collected from clinical exams and caregiver/participant surveys. Evaluation of data collected will be used to determine the effectiveness of the intervention.

NCT ID: NCT02002728 Completed - Clinical trials for Dental Caries in Children

Comparison of Early Caries Detection in Children Utilizing an Electrical Conductance Device and the Gold Standard of Visual-tactile Technique.

Start date: November 2006
Phase: N/A
Study type: Observational [Patient Registry]

The purpose of this study is to evaluate a methodology for detecting early forming cavities in children that is more accurate and reliable than the gold standard used by dentists around the world. The new method uses an electrical current device to detect early enamel mineral loss before it can develop into a cavity. The manual gold standard is for a dentist to probe the surfaces of the teeth with a fine pick, searching for areas of defect.

NCT ID: NCT01978041 Completed - Dental Caries Clinical Trials

Fluoride Bioavailability After Ingestion of Water or Foods Prepared With Fluoridated Water

Start date: January 2013
Phase: Phase 1
Study type: Interventional

The importance of fluoridated water to control caries is well recognized. Although the mode of action of fluoridated water is known (related to a slight increase in fluoride concentration in saliva/dental biofilm in individuals living in fluoridated areas), the kinetics of fluoride concentration in saliva after ingestion of food prepared with fluoridated water, either from fluoride remaining in the oral cavity after mastication, or from fluoride returning from salivary secretion is not known in details. Therefore, the aim of this study is to assess fluoride bioavailability after ingestion of food prepared with fluoridated water. The study will be in vivo, crossover and double blind, in which 12 adult volunteers will participate. In 4 experimental phases, volunteers will ingest: a. a typical Brazilian meal cooked with non-fluoridated water (<0.1 ppm F); b. a typical Brazilian meal cooked with fluoridated water (1 ppm F); c. non fluoridated water (<0.1 ppm F) and d. fluoridated water (1 ppm F). Immediately before and 5, 10, 15, 30, 45, 60, 120, 180 minutes after the ingestion, a blood sample will be collected by digital puncture, and a sample of unstimulated saliva will be collected. Fluoride concentration in the samples will be determined by an ion specific electrode adapted for microanalysis. Results will be analyzed by ANOVA, with significance limit of 5%.