Effect of Modeling Resin on Anterior Direct Composite Veneer (NCT06485024) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Effect of Modeling Resin on Anterior Direct Composite Veneer
25 participantsStarted 2024-07
Plain-language summary
the study will be conducted to evaluate the clinical performance of direct Nanohybrid resin composite veneer restorations applied with or without modeling resin
Who can participate
Age range18 Years – 45 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
What they're measuring
1
comparison of Color stability with and without the intervention