Clinical Trials Logo
  1. Home
  2. Caries
  3. NCT04796974

Clinical Evaluation of "Cention Forte" Restorative Material

Caries Clinical Trial

Official title:
Clinical Evaluation of "Cention Forte" Restorative Material in Class I and II Cavities: A Prospective Controlled Clinical Trial up to 3 Years

Clinical Trial Summary

Resin composites, the first choice of material for the restoration of posterior teeth, still have several drawbacks including their polymerization shrinkage and potential failure of the resin-dentin interface leading to secondary caries. Time-saving and simplified restorative procedures are an ongoing demand for posterior applications.The bulk-fill resin based composites (BF-RBCs), has been developed with an attempt to speed up the restoration process by enabling up to 4- or 5-mm thick increments to be cured in one step. The photo-polymerized single-step BF-RBC materials seem to have some limitations in terms of adequate polymerization. Therefore, recently, the use of dual-polymeritzed RBCs that are also suitable for bulk-fill application with additional bioactive properties such as acid-neutralizing ion release has been offered as an alternative to photo-polymerized ones. Cention N (Ivoclar Vivadent, Schaan, Liechtenstein) restorative material is one approach that has been introduced as a new material category for this purpose. The hand mixed form is named as Cention N whereas auto-mixed capsule form is Cention. Both of them are resin based composite materials categorised as 'alkasite'. They are self-curing composites with optional photo-polymerzation for full volume (bulk) placement. Their composition is same with only exception of the concentration of the initiators and the powder liquid proportion. Cention is delivered together with Cention Primer to ensures the retention of the filling independent of the preparation. The objective of this prospective clinical trial is to evaluate the clinical performance of Cention and Cention Primer in restoration of Class I and II cavities.

Clinical Trial Description

The aim of the study is to place at least 90 posterior restorations with Cention (in at least 45 patients). The patients will be informed about the study and ask to sign the Informed Consent. After having the initial radiographs and images, the preperation will be performed by standard procedures. As the cavity preparation is finished the measurement of the cavity dimensions will be performed by using a periodontal probe. After having the cavity images the cavity will be restored by Cention according to the manufacturer's instructions. Following the occlusal adjustment final image of the restoration will be taken. After 2 weeks the patient will be recalled in order to asses the baseline FDI criteria by two observers. This recall appointment will be done annually up to 3 years. ;

Study Design

Related Conditions & MeSH terms

  • Caries
  • Unsatisfactory or Defective Restoration of Tooth
Clinical Trial Details
NCT number NCT04796974
Study type Interventional
Source Istanbul Medipol University Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date March 8, 2021
Completion date March 8, 2024
View Details
See also
  Status Clinical Trial Phase
Active, not recruiting NCT05311657 - Oral Health and Severe COPD
Completed NCT01529606 - Cold Plasma for Dental Restoration and Caries Prevention N/A
Completed NCT06072742 - Effect of Lifestyle on Caries and Apical Periodontitis
Completed NCT04679558 - Antibacterial Effect of Chlorhexidine Added to the Preventive Protocol in Adolescent Special Needs Early Phase 1
Active, not recruiting NCT04933123 - Clinical Evaluation of a Dental Glass Ceramic in the Indirect Restorative Therapy N/A
Withdrawn NCT02202304 - The Effects of Chlorhexidine/Thymol Varnish on Partial Denture Patient Phase 4
Not yet recruiting NCT04889196 - The Efficiency and Gingival Health Status of Hall Versus SDF Techniques in the Management of Carious Primary Molars Phase 3
Active, not recruiting NCT04708223 - Prospective, Split-mouth, Comparative Study to Compare Clinical Outcomes of Two Different Posterior Composite N/A
Completed NCT06140745 - Evaluation of Dentifrice Formulations to Remineralize Enamel and Dentine Subsurface Lesions in a Double-Blind In-Situ Clinical Trial N/A
Recruiting NCT05144711 - Management of Deep Carious Lesions in Adults N/A
Not yet recruiting NCT03656432 - Effect of CPP-ACP With/Without Fl on White Spot Lesion,Salivary pH and fl Release in High Caries Risk Patients Phase 3
Not yet recruiting NCT02933463 - Clinical Effectiveness of Embrace Wetbond and Clinpro as Pits and Fissure Sealants in Young Permanent Molars N/A
Completed NCT02998814 - Clinical Follow Up of a Fissure Sealant Placed With Different Adhesive Protocols: 2-Year Randomized Split Mouth Study N/A
Completed NCT02027597 - Improving Oral Health With Serious Games N/A
Not yet recruiting NCT05064566 - Evaluation of Caries Detection Methods
Completed NCT06010732 - In Situ Comparison of the Remineralization Potential of Optimized Fluoride Dentifrice With Control Fluoride Dentifrice Phase 3
Recruiting NCT05211843 - Saliva Insulin as Biomarker of Risk Factors for Metabolic Dysregulation and Caries N/A
Not yet recruiting NCT05070416 - Lithium Disilicate Crowns Study N/A
Completed NCT02418520 - The Effect of Miswak Chewing Sticks on the Oral Helicobacter Pylori Infection N/A
Completed NCT04286256 - Using Motivational Interviewing To Reduce Parental Risk-Related Behaviors For Early Childhood Caries N/A