ClinicalTrials.Veeva

Menu

Comparison Between Direct Composite and Indirect Ceramic Laminate Veneers in Multiple Diastema Closure Cases

P

Prince Sattam Bin Abdulaziz University

Status

Completed

Conditions

Dental Leakage

Treatments

Procedure: Indirect technique
Procedure: Direct technique

Study type

Interventional

Funder types

Other

Identifiers

NCT06377423
A54678775

Details and patient eligibility

About

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.

Full 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.

Enrollment

28 patients

Sex

All

Ages

20 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients needed diastema closure.
  • Patients with normal and full occlusion.
  • Patients must have a good oral hygiene.
  • Patients with a tooth respond positively to an electric pulp tester.

Exclusion criteria

  • High caries risk patients with extremely poor oral hygiene.
  • Patients with periodontally-involved teeth.
  • Patients with heavy bruxism habits and clenching.
  • Patients involved in orthodontic treatment.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

28 participants in 2 patient groups

Estelite esteria composite
Experimental group
Description:
Half of the patients received composite veneers using direct method
Treatment:
Procedure: Direct technique
IPS Emax press ceramic
Experimental group
Description:
Half of the patients received ceramic veneers using indirect technique
Treatment:
Procedure: Indirect technique

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems