Clinical Trials Logo

Dental Caries clinical trials

View clinical trials related to Dental Caries.

Filter by:

NCT ID: NCT03827889 Suspended - Dental Caries Clinical Trials

Efficacy of Two Protocols for Applying Fluorine Varnish to Deciduous Teeth

CEPECO3
Start date: January 1, 2024
Phase: N/A
Study type: Interventional

Evidence that the data flow analysis tests, there are still no studies that show the clarity of the protocols of its application, including the interval and execution factors of applications, concentration of fluoridation and previous prophylaxis. That is, there are still large gaps regarding fluoride varnish applications. Thus, the objective of the present project is the selection of two protocols for application of fluid applications in active drugs in primary tooth enamel. The longitudinal follow-up will be performed in a period of 3, 6, 12, 18 and 24 months after the procedure. The progression of a subject will be evaluated clinically through the transition of ICDAS scores and assessment of the lesions (sound examination with superficial measurements) by visual examination, and the physician evaluates the efficacy and the ability to evaluate the therapeutic techniques and evaluation. treatment, cost and quality of life of participants

NCT ID: NCT03823612 Recruiting - Clinical trials for White Spot Lesion of Tooth

Reminerlization Potential of Innovative Biomimetic Material in Caries White Spot Lesions

Start date: March 1, 2019
Phase: Phase 4
Study type: Interventional

to remineralize the white spot caries lesions after orthodontic treatment , the investigator will use two different materials ( Clinpro tooth creme versus Gc tooth mousse) and will compare between their effects in remineralization of white spot caries lesions.

NCT ID: NCT03822403 Completed - Dental Caries Clinical Trials

Clinical Performance Evaluation of a Glass-ionomer Restorative System Evaluation

Start date: May 1, 2009
Phase: N/A
Study type: Interventional

The aim of this clinical trial was to compare the clinical performances of a glass ionomer restorative system with a micro hybrid resin based composite in class I and class II cavities. A total of 140 (80 class I and 60 class II) lesions in 59 patients were restored with a glass ionomer restorative system (Equia) or a micro hybrid composite(Gradia Direct). Restorations were evaluated at baseline and yearly during 9 years according to the modified-USPHS criteria. Data were analyzed with Cohcran's Q and McNemar's tests (p<0.05).

NCT ID: NCT03819868 Recruiting - Dental Caries Clinical Trials

Efficacy of Sealing Molars: Split-mouth Randomized Clinical Trial

Start date: August 15, 2017
Phase: N/A
Study type: Interventional

The sealing of fossae and fissures is an effective procedure in preventing occlusal caries lesions. However, there are gaps regarding its efficacy in the treatment of initial enamel lesions. In addition, there are no studies in the literature that have compared the longevity of sealings performed with the different sealants available in the market. Thus, the objective of this study is to evaluate the efficacy of fossae and fissures sealings performed with a low-cost resinous sealant in occlusal lesions in enamel in permanent and deciduous molars. This is a multicenter clinical study of non-inferiority, randomized, controlled, double blind (patient and operator) with 60 deciduous molars and 340 permanent molars of children 4 and 9 years of age. The sample unit will be the tooth, which will be randomized into two groups using a distributed randomization list in mixed envelopes that will be open only at the time of the procedure. The teeth allocated in the test group will be treated with the sealant preventâ; Those allocated in the control group will employ the Fluroshieldâ sealant. In both groups the procedure will follow the manufacturer's standards. The efficacy of the sealant will be evaluated by means of clinical and radiographic control at 6, 12 and 18 months after the procedure. Secondary outcomes, such as retention, cost, acceptability and quality of life, will also be evaluated.

NCT ID: NCT03817437 Completed - Tooth Decay Clinical Trials

Correlation Study Between Socio-economical Deprivation and Oral Health in Children of 9 Years of Age

PRECA-6
Start date: January 1, 2019
Phase:
Study type: Observational

Retrospective, observational cohort study. Objectives : To search for correlations between socio-economical deprivation and oral health in french children of 9 years of age. To study the annual use of oral and dental care of children from 6 to 9 years of age depending on their geographical and socio-economical environment, and the medical demography ; To identify and study the share of the cohort not using oral and dental care, and the socio-economical and geographical factors implicated in this non-use of care. The study will use data from the french nationwide healthcare systems database (SNDS) and data from the french national institute of statistics and economic studies (INSEE).

NCT ID: NCT03802669 Completed - Dental Caries Clinical Trials

Molecular Assessment of Oral Mutans Streptococcus Isolated From Different Patients

Start date: January 12, 2019
Phase:
Study type: Observational

90 saliva samples will be isolated from patient who possess different ages and caries activity, attending outpatient clinic of October University of Modern Sciences and Arts. Then the determination of the best selective media for mutans streptococcus isolated from saliva and authenticate the MS via PCR technique.

NCT ID: NCT03800043 Completed - Clinical trials for Dental Caries in Children

Social Impact of Children's Dental Appearance

Start date: January 15, 2019
Phase:
Study type: Observational

This study evaluates the social impact of children's dental perception from children with or without caries experience. For this, children and their parents are shown pictures of child faces with healthy teeth, decayed teeth and teeth after dental treatment.

NCT ID: NCT03791255 Not yet recruiting - Clinical trials for Indirect Pulp Treatment

Light Cured Resin Modified Calcium Silicate Versus Light Cured Calcium Hydroxide in Indirect Pulp Treatment of Primary Molars

Start date: February 2019
Phase: Phase 4
Study type: Interventional

The objective of this study is to explore if light cured resin modified Calcium silicate could result in better clinical and radiographic success if compared to light cured Calcium hydroxide when used in indirect pulp capping treatment in primary molars.

NCT ID: NCT03788616 Completed - Dental Caries Clinical Trials

Fluoride Release,Compressive Strength and Clinical Performance of a Bioactive Restorative Material in ART

Start date: November 17, 2018
Phase: Phase 3
Study type: Interventional

The study will be two parallel group, triple blinded randomized controlled clinical trial that based on CONSORT (consolidated standards of reporting trials) guideline .The selected participants according to inclusion and exclusion criteria will be randomly allocated in two groups using (Research Randomizer Program) .

NCT ID: NCT03785769 Withdrawn - Dental Caries Clinical Trials

Pre-etching of Dentin Before Restorations With High Viscosity Glass Ionomer Cement

CEPECO4
Start date: January 1, 2022
Phase: N/A
Study type: Interventional

The objective of this randomized clinical trial is to evaluate the survival of restoration with high viscosity glass ionomer cement (HVGIC) with pre-etching with polyacrilic acid compared with no pre-etching in order to treat occlusoproximais caries lesion in primary molars, as well as the impact of those treatments in the caries lesion progression, the cost-efficacy of the procedures and the discomfort reported by the patient. Children of 4 to 8 years will be selected in the Pediatric Dentistry Clinic of Universidade Ibirapuera. 192 teeth will be randomized in 2 experimental groups: (1) HVGIC restoration with pre-etching and (2) HVGIC restoration with no pre-etching. Will be considered as primary outcome the survival of the restoration evaluated after 6, 12, and 24 months by two trained examiners. The carious lesions progression will be evaluated after 24 months of follow-up. The time of the treatments and the cost of the materials will be considered to estimate the cost-efficacy of each treatment. The discomfort reported by the participant will be measured after each procedure following the Wong-Baker scale. For the primary outcome, Kaplan-Meier survival and the Long-Rank test will be used in order to compare the two groups. Cox regression will be performed in order to evaluate thee influence of explanatory variables on the outcome.