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Dental Caries clinical trials

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NCT ID: NCT00612469 Completed - Dental Caries Clinical Trials

The Use of Antimicrobial Agents in the Inhibition of Mutans Streptococci in Children With Dental Caries

Start date: October 2005
Phase: N/A
Study type: Interventional

The aim of the present study was to compare salivary MS levels in four different groups of children with caries, that have been submitted to intraoral topical treatment with either 1,23% sodium fluoride, 1% chlorhexidine, 3% or 10% vancomycin, during 6 consecutive days. This clinical trial was designed to test two different hypotheses. First, that topical vancomycin would be more effective than chlorhexidine and sodium fluoride in salivary MS reduction. Secondly, a 6-day antimicrobial treatment with either one of these agents would produce a long lasting MS suppression, dispensing repeated antibacterial treatments.

NCT ID: NCT00541060 Completed - Dental Caries Clinical Trials

Study of Factors of Genetic Susceptibility Associated to Severe Caries Phenotype

Cariogene
Start date: October 2007
Phase: N/A
Study type: Interventional

Alteration of the post- eruptive enamel microstructure due to a mutation of a gene coding for a matrix protein could increase the susceptibility of the enamel to caries after tooth eruption. To identify in young patients with severe caries incidence, the occurrence of mutations in several candidate genes which result in an alteration of the enamel microstructure that could explain the high caries susceptibility of the patient.

NCT ID: NCT00526422 Completed - Dental Caries Clinical Trials

DPBRN Assessment of Caries Diagnosis & Caries Treatment

Start date: February 2006
Phase: N/A
Study type: Observational

The purpose of this study was to determine what methods Dental PBRN dentists use for diagnosis, prevention, and treatment of dental decay.

NCT ID: NCT00497029 Completed - Dental Caries Clinical Trials

Early Childhood Caries Prevention at a Pediatric Clinic

Start date: June 2004
Phase: N/A
Study type: Interventional

This purpose of this study was to evaluate effectiveness of a risk-based dental caries prevention program conducted by dental personnel at an urban pediatric primary care clinic serving largely low-income residents of Baltimore, Maryland, and to appraise this program as a model for similar urban pediatric settings.

NCT ID: NCT00495495 Completed - Dental Caries Clinical Trials

Healozone Study to Evaluate the Safety and Efficacy of the Use of Ozone for Management of Dental Caries

Start date: February 2007
Phase: Phase 2/Phase 3
Study type: Interventional

Caries means demineralization with the formation of cavities and pulp symptoms and necrosis as an end result. The acids in the mouth are mainly produced by oral bacteria like Streptococcus mutans from bacterial biofilms adhering to the tooth. Ozone has been shown to have a very strong bactericidal effect on bacteria causing dental caries. Baysan et al reported that there was a statistically significant reduction of streptococci in root caries lesions and saliva samples after ozone application. The positive clinical effect of ozone with respect to arresting caries progression and the remineralization of caries has been shown in vitro and in vivo. In an in vivo study, Baysan and Lynch found that the application of ozone resulted in a significant reduction of bacterial contamination as well as a reduction in size and severity of root caries lesions. In a subsequent study, Baysan and Lynch reported that the severity of root caries lesions was significantly reduced after ozone application as measured by electrical conductance and laser fluorescence. In several studies, the caries reducing effect of ozone was measured with biochemical methods in root surface caries lesions, the biofilm and saliva after ozone application. See Citation section for references. The objectives of this multi-center clinical study were to determine: (1) the effectiveness of the HealOzone in stopping the progression of fissure caries; and (2) the oral soft tissue safety of the ozone system.

NCT ID: NCT00490165 Completed - Diabetes Clinical Trials

Periodontal and Periapical Inflammation and Pregnancy

Start date: March 2007
Phase: N/A
Study type: Observational

This is a retrospective chart review of patient records at the University of Mississippi Medical Center. We are not actively recruiting patients for this study. Recent animal studies we conducted showed that periapical abscesses during pregnancy cause a systemic inflammatory response in the mother. Also due to the increase in TNF-alpha (an inflammatory cytokine) the mother also become insulin resistant and thus developed gestational diabetes. Periodontal inflammation has been shown in the research to lead to low-birth weight and pre-term birth. We are looking retrospectively to see if an association exists in charted data between periapical and periodontal inflammation and adverse pregnancy outcomes.

NCT ID: NCT00482573 Completed - Pregnancy Clinical Trials

Dental Anesthesia in Pregnant Women With Rheumatic Heart Disease

Start date: April 2004
Phase: Phase 1
Study type: Interventional

The hemodynamic parameters of 31 pregnant women with rheumatic valve disease, undergoing restorative dentistry under local anesthesia with 2% solution of lidocaine, divided in two groups, with (Group LE) and without 1:100,000 epinephrine solution (Group LNE), were studied by 24-hour ambulatory electrocardiographic monitoring, intermittent blood pressure monitoring and continuous cardiotocography, during three standard time periods. A significant decrease in the values of maternal heart rate was seen during the procedure, in comparison with the other two time periods in the two groups, as well as, the occurrence of cardiac arrhythmia in 9 (29.1%) patients, being 7 (41.8%) of them in the group receiving epinephrine anesthesia. We conclude the use of 2% lidocaine in association with epinephrine proved safe during dental procedure in pregnant women with rheumatic valve disease.

NCT ID: NCT00475618 Completed - Dental Decay Clinical Trials

Effect of Therapeutic Measures in Dental Caries Reduction in Children With Primary Dentition From Medellín City

Start date: May 2007
Phase: Phase 3
Study type: Interventional

The propouse of this study is to evaluate some combined preventive measures, of easy application in children under 6 years old as education, brush teeth, fluoride free tooth paste,fluoridated tooth paste, professional cleaning and fluoride varnish application, to determine between three groups of differents combined preventive measures, wich one is better in reduting dental caries appearance. Hypothesis: 1. Ho: Dental caries reduction percentage is larger or equal in the group with only prevention education and Professional cleaning, than in the groups intercepted with fluoride varnish or fluoride toothpaste. 2. Ha: Dental caries reduction percentage is less in the group with only prevention education and Professional cleaning, than in the groups intercepted with fluoride varnish or fluoride toothpaste.

NCT ID: NCT00464009 Completed - Clinical trials for Early Childhood Dental Caries

Development and Evaluation of a Medical Intervention for Early Childhood Caries

IMB-RCT
Start date: February 2001
Phase: N/A
Study type: Interventional

This study aimed to evaluate the effect of three forms of continuing medical education (CME) on provision of preventive dental services to Medicaid-enrolled children by medical personnel in primary care physician offices.

NCT ID: NCT00393055 Completed - Dental Caries Clinical Trials

Xylitol Adult Caries Trial (X-ACT)

Start date: January 2007
Phase: Phase 3
Study type: Interventional

The purpose of the trial is to determine the extent to which daily use of xylitol lozenges reduces the appearance of new caries lesions in adults who tend to experience such lesions (i.e., caries-active adults).