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Carious Teeth clinical trials

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NCT ID: NCT06226389 Active, not recruiting - Carious Teeth Clinical Trials

Clinical Evaluation of Different Bulk-fill Composite Restorations on Posterior Teeth

2-Year
Start date: January 17, 2024
Phase: N/A
Study type: Interventional

Different bulk-fill composites will be applied in different posterior cavities then compared

NCT ID: NCT06161103 Not yet recruiting - Carious Teeth Clinical Trials

Comparison of 3D Printed Composite Resin Crowns With Stainless Steel Crowns

Start date: November 30, 2023
Phase: N/A
Study type: Interventional

The goal of this splith - mouth clinical trial is to compare 3D Printed Prefabric Composite Resin Crowns with Stainless Steel Crowns in healthy 50 children age between 5 and 9 with caries on more than one surface of the primary second molars. The main question[s] it aims to answer are: - 3D printed composite resin crown's survival rate is as succesful as stainless steel crowns - 3D printed composite resin crowns periodontal integrity is as succesful as stainless steel crowns Condition or disease : Carious Teeth Intervention/treatment: Procedure/Surgery: 3D Printed Prefabricated composite resin crown group Procedure/Surgery: Prefabricated stainless steel crown group

NCT ID: NCT06101550 Not yet recruiting - Carious Teeth Clinical Trials

Evaluation of Partial Versus Complete Pulpotomy in Carious Immature Young Permanent Teeth Using Bioceramic Material

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

One of our major concerns and daily challenges is the management of carious immature permanent teeth, also known as young permanent teeth while preserving the vitality of the dental. Preserving radicular pulp tissue in these teeth allows continuing apical maturation and apical closure. Diagnosis and treatment of carious immature permanent molars are considered a challenging aspect of daily clinical routine, where constant irritation of the pulp without treatment leads to irreversible pulpitis and necrosis, which impedes the natural root development and its complete formation ; leading at the end to a decision of extracting the tooth .Therefore; when treating immature permanent teeth, the main goal is to preserve the vitality of the pulp to guarantee natural root development. Pulpotomy is a commonly employed treatment for this procedure involving either the removal of only the outer layer of damaged and hyperemic tissue in exposed pulps (partial pulpotomy or Cvek pulpotomy); which is a procedure staged between pulp capping and complete pulpotomy. Complete pulpotomy is the total removal of coronal pulp tissue and the placement of a wound dressing on the canal orifice. Followed by the placement of a biocompatible material to promote healing and regeneration of the remaining vital pulp tissue. In many studies, MTA showed high success rates in treatment of carious immature permanent molars. However, MTA is expensive and has poor handling characteristics, a long setting time and no predictable antimicrobial activity. Recently, new bioceramics have emerged as promising materials, showing good potential for vital pulp therapy in immature permanent teeth due to their biocompatibility and favorable clinical outcomes. Both MTA and bioceramics have almost similar compositions, but bioceramics materials contain titanium oxide and calcium phosphate, in addition to the absence of aluminum in its composition. Besides, bioceramics can release a high percentage of calcium ions early while maintaining this high percentage for 28 days, in contrast to the mineral trioxide, which showed a lower ability to release calcium ions more slowly. Therefore, this study will be conducted to compare the effectiveness bioceramic material in partial and complete pulpotomy of immature permanent molars.

NCT ID: NCT05910905 Not yet recruiting - Carious Teeth Clinical Trials

Clinical Efficacy of Preformed Pediatric Zirconia and Metal Crown

Start date: July 1, 2023
Phase: N/A
Study type: Interventional

The study was planned to evaluate and compare the clinical success of prefabricated stainless steel crowns and zirconia crowns used in the primary molars. The study will be carried out in healthy children aged 6-9 years with caries on more than one surface of the primary molars.

NCT ID: NCT05500547 Completed - Carious Teeth Clinical Trials

Clinical Performance of One-shade Universal Dental Resin Composite as Posterior Restoration

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

This study is aimed to evaluate the clinical performance of new One-shade universal composite resin as posterior restoration using US Public Health Service "USPSH" criteria for color match, marginal adaptation, surface texture, retention, recurrent caries and others after 1, 3, 6 and 9 months.

NCT ID: NCT05281861 Active, not recruiting - Adaptation Clinical Trials

Marginal Evaluation of Zirconia Reinforced Lithium Disilicate Partial Coverage Restoration of Egyptian Posterior Teeth.

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

Objective: To evaluate the marginal adaptation of the zirconia reinforced lithium disilicate (VITA AMBRIA) glass ceramic Inlay/Onlay compared with lithium disilicate(IPS emax Press) glass ceramic Inlay/Onlay in decayed posterior teeth.

NCT ID: NCT05265104 Completed - Carious Teeth Clinical Trials

Laser Versus Silver Diamine Fluoride in Hall Technique in Primary Teeth

SDF
Start date: March 10, 2021
Phase: N/A
Study type: Interventional

The hall technique for primary teeth depends on the idea of isolation of the carious non exposed primary tooth from all bacteria present in the oral cavity by using a stainless-steel crown which result in arresting of the caries and preventing its progress to the pulp. Recently laser and Silver Diamide Fluoride (SDF) have been used to arrest the progress of caries so in the current study we will compare the success rate of hall technique with either laser or SDF in arresting of caries

NCT ID: NCT04438642 Enrolling by invitation - Carious Teeth Clinical Trials

Biological and Esthetic Evaluation of Ceramic Onlay With Different Preparation Designs

Start date: November 9, 2019
Phase: N/A
Study type: Interventional

Aim of study: is to asses biological and esthetical success of ceramic onlay restorations while preparing the teeth using shoulder finish line preparation versus butt joint with bevel preparation. Methods: Patients with need to posterior onlay restoration (premolars and molars) will be allocated into two groups either conventional (shoulder finish line) or conservative group (butt joint with bevel), after tooth preparation impression, restoration fabrication, try in, cementation and restoration will be evaluated two weeks post cementation then follow up will be held every two months for 1 year.

NCT ID: NCT04345263 Active, not recruiting - Carious Teeth Clinical Trials

Outcome of Full Pulpotomy Using Calcium Silicate Based Materials

pulpotomy
Start date: September 1, 2017
Phase: N/A
Study type: Interventional

Permanent teeth with carious pulp exposure and indicated for full pulpotomy will be treated using three different materials using aseptic technique and will be subsequently followed up clinically and radiographically at 6 months, 1 year and yearly up to 5 years.

NCT ID: NCT02915419 Not yet recruiting - Carious Teeth Clinical Trials

Evaluation of Survival of Mature Second Premolar Treated With Regenerative Techniques

Start date: October 2016
Phase: N/A
Study type: Interventional

This study aims to compare the ability of different regenerative protocols in the treatment of mature necrotic