Clinical Trials Logo

Clinical Trial Summary

Thus, the present study aimed to evaluate the longevity of direct composite compared to indirect ceramic laminate veneers in multiple diastema closure cases using USPHS criteria. The formulated null hypothesis was that there is no significant difference in the clinical performance of direct composite and indirect ceramic laminate veneers in multiple diastema closure cases over two years.


Clinical Trial Description

Restorative materials and curing device In the current study, the manufacturer's instructions were followed for the use of the nanofilled composite resin (Estelite Asteria, Tokuyama Dental, Japan) for direct laminate veneers and IPS e.max Press (Ivoclar Vivadent, Amherst, NY, USA) for indirect laminate ceramic veneers. A light curing device with an output density of 655 mW/cm2 (LED Bluephase C5, Ivoclar, Vivadent, Amherst, NY, USA) was used. Demetron LED light meters were used to measure the light curing unit's intensity regularly (Demetron Research Corp., Danbury, CT, USA). Brand name, description, chemical composition, and manufacturers of the materials are presented in Table 1. Study design, blinding & randomization The Consolidated Standards of Reporting Trials statement was adhered to in the description of the experimental design. This study was a randomized controlled clinical trial that was double-blinded for both trial participants and outcome assessors. Randomization was performed using the flip of a coin for the choice of material. Using computerized sequence generating (www. randomizer.org), participants were divided into two groups with a 1:1 allocation ratio. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06377423
Study type Interventional
Source Prince Sattam Bin Abdulaziz University
Contact
Status Completed
Phase N/A
Start date August 1, 2021
Completion date January 10, 2024

See also
  Status Clinical Trial Phase
Completed NCT04848987 - Indirect Resin Composite Inlays Cemented With a Self-adhesive, Self-etch or a Conventional Resin Cement N/A
Completed NCT04679220 - 36-Months Clinical Evaluation of Preheated and Room Temperature Resin Composite N/A
Recruiting NCT05383768 - Clinical Evaluation of Preheated and Repeated Preheated Versus Conventional Bulk Fill Resin Composite N/A
Completed NCT03542019 - Survival of Endocrowns Made From Different Ceramics N/A
Not yet recruiting NCT03886727 - Effectiveness of Rubber Dam Isolation Versus Cotton Roll Isolation on Bonded Fissure Sealant Retention N/A
Completed NCT05161559 - Adhesive Performance of Glass Ionomer and Resin Based Adhesive Systems: A 3 Years Prospective Clinical Evaluation N/A