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NCT ID: NCT04010929 Completed - Pulpotomy Clinical Trials

Efficacy of Er,Cr:YSGG Laser in Partial Pupotomy

Start date: January 8, 2018
Phase: N/A
Study type: Interventional

The aim of this study was to compare the efficacy of partial pulpotomy treatment using MTA and Er,Cr:YSGG + MTA in permanent immature molar teeth with deep dentin caries. The study was performed in children aged between 6-15 who had at least one deep dentine caries in permanent immature molar tooth. The patients' therapies were completed in Kırıkkale University, Faculty of Dentistry, Department of Pediatric Dentisry. A total of 90 teeth (caries exposed) were included in the study. According to the treatment, the teeth were randomly divided into two groups: 1. MTA group (n=45), 2. Laser+MTA group (n=45). In the MTA group, after removing caries, MTA was applied to the exposed area on the pulp following bleeding control with 5.25% NaOCl. In the same session, the tooth was restored with resin modified glass ionomer cement and composite resin. In the laser+MTA group, the treatment procedures were the same as the MTA group, and before the MTA condensation, Er, Cr: YSGG laser was applied to the exposure area after bleeding control to provide biostimulation. Patients were called for followup appointments at 1, 3, 6 and 12 months after treatment and control radiographs were taken.

NCT ID: NCT03443583 Completed - Adhesion Clinical Trials

Immediate and Delayed Dentin Sealing Effect on Partial Crowns

Start date: November 1, 2013
Phase: N/A
Study type: Interventional

Immediate Dentin Sealing as an adjunct to adhesive cementation of all ceramic restorations is proposed and executed in several studies, but there is very limited evidence to support its effectiveness. It is presumed that IDS both reduces postoperative sensitivity and increases the bond strength to dentin as compared to DDS.

NCT ID: NCT03430713 Completed - Color Perception Clinical Trials

Comparison of Visual and Spectrophotometric Methods for Dental Color Measurement - An in Vivo Study

Start date: January 2017
Phase: N/A
Study type: Interventional

Twenty patients of Dental Medicine School will be recruited to participate in a pilot study about dental color measurement in which visual and digital instruments will be tested. Informed consents and local ethical committee clearance will be previously obtained. All data will be collected after an oral hygiene procedure. Two different methods of color measurement will be tested: visual method with VITA Classical (VC) and VITA 3D-Master (VM) and digital method with Spectroshade Micro (SS) and VITA Easyshade (ES). The CIE L*a*b* values will be evaluated in the VC scale for both methods. Reproducibility will be assessed based on intra-operator intra-device agreement and the accuracy will be assessed based on inter-device agreement using the kappa coefficient (K) and intraclass correlation coefficient (ICC), respectively. Results will be presented as mean, with 95% CI

NCT ID: NCT01805869 Recruiting - Tooth Diseases Clinical Trials

Oral Specimen and Data Acquisition Study of Subjects Requiring Third Molar Removal

Start date: June 19, 2013
Phase:
Study type: Observational

Background: - The third molars (wisdom teeth) normally grow in during late adolescence or early adulthood. Many people need or choose to have these teeth removed with oral surgery. Normally, the removed teeth and tissue are thrown away as medical waste. However, oral health researchers want to collect the teeth and tissue for research. They also want to encourage dentists at the National Institutes of Health to improve their skills in oral surgery. This study will collect the teeth and tissue of people who need to have oral surgery to remove their wisdom teeth. Objectives: - To provide continued dental skills training for dentists at the National Institutes of Health. - To collect teeth and tissue samples following wisdom tooth removal surgery. Eligibility: - Individuals between 16 and 50 who need to have their wisdom teeth removed. Design: - This study will involve a minimum of three visits. There will be a screening visit, a surgery visit, and at least one follow-up visit. - Participants will be screened with a physical exam and medical history. A full dental exam with x-rays will be given to evaluate the need for surgery. - At the second visit, participants will have oral surgery to remove their wisdom teeth. The teeth and tissue removed during the surgery will be collected for study. - Participants will receive drugs to control the pain after surgery. They will also be able to contact a dentist if there are any problems. - Between 7 and 21 days after surgery, participants will have a followup visit to check the healing. If they are having no problems, this will be the last visit. If there are any postsurgery issues, they will be scheduled for additional visits as needed.