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Tooth Disease clinical trials

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NCT ID: NCT06315816 Recruiting - Anxiety and Fear Clinical Trials

Virtual Reality Used During Tooth Extraction and Extirpation Treatment

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

This study carriy out to evaluate the effect of virtual reality glasses used during tooth extraction and extirpation treatment under local anesthesia on anxiety and fear in children aged 7-10 years.

NCT ID: NCT05711511 Recruiting - Tooth Disease Clinical Trials

Radiographic Comparison of Obturation Performed by Conventional Method and Obtura II.

Start date: August 27, 2022
Phase: N/A
Study type: Interventional

Root canal therapy plays an importanmt role in dental health care.An importanat parameter necessary to achieve a proper endodontic treatment is quality of root canal filling.This study compare the radiographic quality of obturation with cold lateral condensation and thermoplasticiszed gutta percha technique and obtura II system.

NCT ID: NCT04825379 Active, not recruiting - Tooth Disease Clinical Trials

Clinical Evaluation of a Bioactive Material

Start date: June 1, 2021
Phase: N/A
Study type: Interventional

The clinical performance of a bioactive composite and a posterior resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 2 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into two groups: a bioactive composite [Cention N, Ivoclar Vivadent, Schaan, Liechtenstein (CN)] and a posterior resin composite [G-ænial Posterior (GC, Tokyo, Japan) (GP)] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using FDI criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

NCT ID: NCT04685967 Active, not recruiting - Tooth Disease Clinical Trials

Clinical Evaluation of a Restorative Glass Ionomer and a Bulk-fill Composite Resin

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

The clinical performance of a restorative glass ionomer and bulk-fill resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 2 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into two groups: a restorative glass ionomer [Equia Forte HT, GC, Tokyo, Japan (EHT)] and bulk-fill composite resin [SonicFill2, Orange, CA, USA (SBF)] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using modified United States Public Health Service (USPHS) criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

NCT ID: NCT04685954 Active, not recruiting - Tooth Disease Clinical Trials

Clinical Comparison of Bulk-fill and Incremental Composite

Start date: March 1, 2018
Phase: N/A
Study type: Interventional

The clinical performance of a 5-mm bulk-fill and an incremental resin composite in class II restorations will be evaluated and compared. After recruiting participants with at least 2 approximal caries lesions, all restorations will be placed by a single clinician. All caries lesions will be removed before restoring. Cavities will be divided into two groups: a 5 mm bulk-fill composite resin [Filtekā„¢ Bulk Fill Posterior, 3M ESPE, St. Paul MN, USA (FB)] and an incremental posterior composite resin [Filtek Ultimate Universal, 3M ESPE, St. Paul MN, USA (FU)] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using modified United States Public Health Service (USPHS) criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

NCT ID: NCT04266210 Active, not recruiting - Tooth Disease Clinical Trials

Clinical Evaluation of a Restorative Glass Ionomer and a Composite Resin for the Restoration

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

The clinical performances of a restorative glass ionomer and a composite resin will be compared in the restoration of non-carious cervical lesions (NCCLs) at patients with systemic diseases. After recruiting participants with at least 2 NCCLs and at least one systemic disease, all restorations will be placed by a single clinician. All lesions will be cleaned before restoring. NCCLs will be divided into two groups: a conventional restorative glass ionomer cement [Fuji Bulk (GC, Tokyo Japan) (FB)] and a posterior composite resin [G-ænial Posterior (GC, Tokyo Japan) (GP)] All restorative procedures will be conducted according to manufacturers' instructions. Restorations will be scored using modified United States Public Health Service (USPHS) criteria after a week (baseline) 6, 12, 24, 36 and 48 months. Descriptive statistics will be performed using chi-square tests.

NCT ID: NCT03423784 Completed - Tooth Disease Clinical Trials

Performance and Tolerability of a New Medical Device Gel, a Randomized, Open Label, Parallel-group, Multicentre Study

Start date: November 15, 2013
Phase: N/A
Study type: Interventional

Medical device study for efficacy and tolerability of a HA gel in the management of teething symptoms

NCT ID: NCT02161874 Completed - Partial Edentulism Clinical Trials

Evaluation of Integration Success and Crestal Bone Preservation Biomet 3i's T3 Implant System

OAK
Start date: April 2013
Phase: N/A
Study type: Interventional

This study evaluates the T3 implant system for the preservation of alveolar crestal bone and the establishment of initial integration. The new surface-treated features of the implant may contribute to improved soft and hard tissue healing. The success rate of the T3 implant will be no different than that of the control implant, which possess similar geometry but different surface treatments.

NCT ID: NCT02158377 Completed - Partial Edentulism Clinical Trials

TM vs TSV Implants Loaded Early vs Conventional in Anterior and Posterior Areas

TMEL
Start date: March 2013
Phase: N/A
Study type: Interventional

Randomized-controlled, multicenter study of Trabecular Metal (TM) and Tapered Screw-Vent (TSV) dental implants loaded early in maxillary and mandibular sites.

NCT ID: NCT01529879 Completed - Partial Edentulism Clinical Trials

Assessment of the Effect of an Implant System With a Novel Abutment Attachment Design on Crestal Bone Preservation

Polaris
Start date: August 2011
Phase: N/A
Study type: Interventional

Integration success rates and the preservation of crestal bone will be higher for the experimental device than for the control implants.