Randomized Clinical Trial on Direct Composite and Indirect Ceramic Laminate Veneers in Multiple Diastema Closure Cases: 2-years Follow-up
Direct technique
+ Indirect technique
Dental Leakage
+ Stomatognathic Diseases
+ Tooth Diseases
Treatment Study
Summary
Study start date: August 1, 2021
Actual date on which the first participant was enrolled.This clinical trial focuses on closing gaps between teeth, known as diastema, using two types of dental veneers: direct composite veneers and indirect ceramic veneers. The study aims to compare the effectiveness and durability of these two materials over a period of two years. The participants in this study are individuals with multiple spaces between their teeth, and the outcomes of this research could help determine which veneer material provides better long-term results, thus improving dental aesthetics and function for those with similar dental issues. Participants in this study are randomly assigned to receive either direct composite veneers or indirect ceramic veneers. The direct veneers are applied directly to the teeth using a nanofilled composite resin, while the indirect veneers involve a ceramic material that is custom-made and then bonded to the teeth. The application process for both types of veneers follows strict procedures using specialized light curing devices to ensure proper bonding. The study is double-blinded, meaning that neither the participants nor the researchers assessing the outcomes know which type of veneer each participant received, which helps to eliminate bias in the results.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.28 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 20 to 35 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location