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Effect of Modeling Resin on Anterior Direct Composite Veneer

Clinical Performance of Direct NanoHybrid Resin Composite Veneer Restorations Applied With or Without Modeling Resin:a Randomized Controlled Trial

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06485024
Enrollment
25
Registered
2024-07-03
Start date
2024-07-31
Completion date
2025-08-31
Last updated
2024-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Decay, Dental Wear

Brief summary

the study will be conducted to evaluate the clinical performance of direct Nanohybrid resin composite veneer restorations applied with or without modeling resin

Detailed description

ChatGPT This study aims to investigate the impact of modeling resin on the clinical performance of direct nanohybrid resin composite veneer restorations in anterior teeth. Resin composites are widely used in dental restorations due to their aesthetic qualities, but issues like discoloration and surface roughness can affect their longevity and patient satisfaction. Modeling resin, used to aid in composite placement and sculpting, has become common, but concerns exist regarding its effects on composite properties, particularly long-term color stability. The research will employ a randomized controlled trial design with a two-arm parallel approach. Adult patients (18-45 years) with anterior tooth defects suitable for composite veneer restoration will be recruited. The intervention group will receive nanohybrid resin composite with modeling resin, while the comparator group will receive the composite without modeling resin. Outcomes will be assessed using modified USPHS criteria, including color stability, color match, anatomical form, marginal adaptation, marginal discoloration, retention rate, presence of secondary caries, and postoperative sensitivity, at baseline and at follow-up intervals of 1, 3, 6, and 12 months. Statistical analysis will involve independent t-tests for intergroup comparisons and repeated measures ANOVA for intragroup comparisons, with a significance level set at 0.05. The study aims to determine if the use of modeling resin influences the clinical outcomes of resin composite veneer restorations. Ethics approval will be obtained, and confidentiality of participant data will be strictly maintained throughout the study period. Overall, this research seeks to provide insights into optimizing the application of resin composites in dental practice to enhance patient outcomes and satisfaction

Interventions

DEVICEModeling Resin

it is the application of Modeling liquid to make easier manipulation and sculpting the composite veneer and reflect on its physical properties and clinical performance

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* • Adults (18-45Ys) with anterior tooth defects indicated for direct composite veneer restoration. * Males or females. * Community-dwelling * Have all his/her anterior teeth with sufficient enamel structure * With ≥ 1 anterior tooth defect * Have sufficient cognitive ability to understand consent procedures * Anterior tooth defect indicated for direct composite veneer * Vital upper or lower anterior teeth with no signs or symptoms of irreversible pulpitis. * Mobility grade: no clinical mobility * Plaque index ≤ 2

Exclusion criteria

* Patients younger than 18 or older than 45 years old • Disabilities. * Systemic diseases or severe medically compromised. * Lack of compliance. * Evidence of severe bruxism, clenching or temporomandibular joint disorders. * Cognitive impairment Periapical pathosis or signs of pulpal pathology. * Malocclusion * Possible prosthodontic restoration within 1 year. * Non-vital tooth. * Endodontically treated tooth. * Severe periodontal affection or tooth indicated for extraction.

Design outcomes

Primary

MeasureTime frameDescription
comparison of Color stability with and without the interventionbaseline and after one yearby using Spectrophotometer to measure the color considering the intervention

Secondary

MeasureTime frameDescription
comparing the effect of the intervention on anatomical formbaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on surface texturebaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on marginal adaptationbaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on color matchbaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on retention ratebaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on postoperative sensitivitybaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on recurrent cariesbaseline and after one yearusing the modefied USPHS criteria
comparing the effect of the intervention on marginal discolorationbaseline and after one yearusing the modefied USPHS criteria

Contacts

Primary ContactSarah A. Azzazy, postgrad
sarah.azzazy@dentistry.cu.edu.eg+02 10 18 300 996
Backup ContactAsmaa A. Yassen, professor
Asmaa.Yassen@dentistry.cu.edu.eg+02 100 191 2610

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026