Clinical Trials Logo

Dental Caries clinical trials

View clinical trials related to Dental Caries.

Filter by:

NCT ID: NCT01268605 Completed - Dental Caries Clinical Trials

Postoperative Hypersensitivity Randomized Comparative Effectiveness Research Trial

POH RCERT
Start date: September 2010
Phase: Phase 3
Study type: Interventional

Postoperative hypersensitivity (POH) is a problem for many patients as determined by the recent Practitioners Engaged in Applied Research and Learning (PEARL) study of POH following occlusal caries restoration. The objectives of this two-armed randomized comparative effectiveness research trial (RCERT) are to determine whether adding a resin modified glass ionomer liner (RMGI) reduces POH in dentin bonded Class I resin based composite (RBC) restorations, and to identify other factors (putative risk factors) that are associated with increased POH. The primary outcome of this study is the reduction/elimination of restoration POH as measured by clinical assessment (air stream) and patient-reports. Outcomes will be ascertained via the following specific aims: Specific Aim 1: To compare the reduction of hypersensitivity of study teeth by clinical measurement (air drying) and by patient-reported outcomes among the two treatment groups at three points in time: prior to restoration and at one and four weeks postrestoration. Specific Aim 2: To identify putative risk factors for POH (or factors associated with differences in POH) including: preoperative caries stage measured by the proposed American Dental Association (ADA) Caries Classification System (CCS), lesion depth as measured on the preoperative radiograph, dentin caries activity ranked on opening the lesion, preparation depth, and patient sleep bruxism status.

NCT ID: NCT01244997 Completed - Dental Caries Clinical Trials

Evaluation of Implants Placed Immediately or Delayed Into Extraction Sites

Start date: November 2003
Phase: Phase 3
Study type: Interventional

IRB4729 Study Hypothesis: Is there a significant difference in the hard and soft tissue response comparing immediate with delayed implant after tooth removal, with immediate provisionalization, in maxillary anterior sites. The purpose of this study is to determine and compare the crestal bone levels as the primary endpoint variable for implants placed and temporized in extraction sites, to implants placed into extraction sites after the extraction site has been grafted and healed for 4 months, all immediately restored with an anatomic provisional restoration.

NCT ID: NCT01205971 Completed - Clinical trials for Dental Caries in Children

Tooth Smart Healthy Start: Oral Health Advocates in Public Housing

Start date: January 2011
Phase: N/A
Study type: Interventional

Dental caries is the most common chronic disease of childhood and is increasing in prevalence in children 2-5 years old. Racial and ethnic minority groups as well as economically disadvantaged individuals are affected the most by this health outcome. This study will test if a community-based multimodal intervention will reduce 2-year incidence of early childhood caries (ECC) in children aged 0-5 living in public housing developments. The intervention combines the components of motivational interviewing (counseling) delivered by dental health advocates, fluoride varnish application, oral health assessment and referral. The investigators hypothesize that the multimodal intervention with motivational interviewing will reduce ECC behavioral risk factors thereby leading to a reduction of ECC incidence when compared to fluoride varnish application, written oral health education materials and oral health assessment and referral.

NCT ID: NCT01201876 Completed - Dental Caries Clinical Trials

DPBRN Reasons for Replacement or Repair of Dental Restorations

Start date: November 2008
Phase: N/A
Study type: Observational

The purpose of this study was to document the reasons for replacement or repair of defective restorations ("fillings") and to record the restorative material of the failed restoration and the material used in the replacement restoration on permanent ("adult") teeth.

NCT ID: NCT01201447 Completed - Dental Caries Clinical Trials

DPBRN Prevalence of Questionable Occlusal Caries Lesions

Start date: August 2008
Phase: N/A
Study type: Observational

The purpose of this study was to investigate the process involved when making decisions about the diagnosis and treatment of questionable lesions, as well as determine if there is any association between lesions progression (or depth, if opened) and clinical characteristics and baseline risk assessment.

NCT ID: NCT01201408 Completed - Dental Caries Clinical Trials

DPBRN Longitudinal Study of Dental Restorations Placed on Previously Un-restored Surfaces

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

The purpose of this study is to assess the quality and expected lifespan of fillings recorded in the DPBRN "Reasons for placing the first restoration on permanent tooth surfaces" study, and the factors affecting how long the fillings last.

NCT ID: NCT01201395 Completed - Dental Caries Clinical Trials

DPBRN Longitudinal Study of Repaired or Replaced Dental Restorations

Start date: September 2009
Phase: N/A
Study type: Observational

The purpose of this study is to assess the quality and expected lifespan of fillings recorded in the DPBRN "Reasons for replacement and repair of dental restorations" study, and the factors affecting how long the fillings last.

NCT ID: NCT01176396 Completed - Dental Caries Clinical Trials

CAMBRA - PBRN Caries Management By Risk Assessment In A Practice-Based Research Network

CAMBRA-PBRN
Start date: April 2012
Phase: N/A
Study type: Interventional

The goal of this project is to create a Practice Based Research Network with 30 researcher dentists calibrated on the administration of a caries risk assessment and the treatment modalities recommended based on the caries risk assessment results (Caries Management by Risk Assessment - CAMBRA), and to conduct a 2-year CAMBRA study in those dental offices. Participating dentists will be a mix of general practitioners and pediatric dentists selected from private practice, part time university faculty, large group practices, or community clinics. Participating practices will collect baseline data and patient progress and report on patient acceptance and compliance, and the effectiveness of treatment. The program's duration is anticipated to be approximately four years. Year one will be dedicated to program, protocol and evaluation design, and recruitment, selection and calibration of researcher dentists. Years two and three will be the research and data collection time period, and year four will be dedicated to evaluation.

NCT ID: NCT01129440 Completed - Dental Caries Clinical Trials

Glass Ionomer Sealant and Fluoride Varnish Study to Prevent Early Childhood Caries

GIFVT
Start date: June 2011
Phase: Phase 2
Study type: Interventional

The goal of this project is to conduct a community-based randomized clinical trial to compare the caries prevention efficacy of fluoride varnish applied every six months vs. fluoride varnish applied every six months and fluoride releasing glass ionomer sealants applied annually to the eligible occlusal surfaces of primary molars in 3-6-year-old children.

NCT ID: NCT01128946 Completed - Dental Caries Clinical Trials

Enamel Remineralization Potential of Dentifrices in Situ

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

This study will use an oral in-situ caries model to study remineralization of enamel due to the action of different combinations of fluoride salts delivered from dentifrices.