Retention & Fracture of Emax Laminate Veneers Clinical Trial
Official title:
One Year Clinical Evaluation of E.Max Laminate Veneers With and Without Using Grape Seed Extract as a Natural Collagen Cross-linking Agent Before Bonding
The aim of this study is to evaluate the clinical performance of E-max veneers cemented with and without using grape seed extract before bonding.
| Status | Not yet recruiting |
| Enrollment | 16 |
| Est. completion date | December 2017 |
| Est. primary completion date | December 2017 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Both |
| Age group | 20 Years to 40 Years |
| Eligibility |
Inclusion Criteria: 1. Patients between 20-40 years old, able to read and sign the informed consent document. 2. Patients having teeth with exposed dentin surface limited to cervical third. 3. Patients, healthy physically and psychologically, able to tolerate conventional restorative procedures. 4. Patients don't have active periodontal or pulpal diseases and have teeth with good restorations. 5. Patients with normal occlusion. 6. Patients with teeth problems indicated for laminate veneer (e.g. discoloration, mild malposition, fracture not involving more than 50% enamel loss, ….) 7. Patients willing to return for follow-up examination and evaluation. Exclusion Criteria: 1. Patients in the growth stage with partially erupted teeth. 2. Patients with fractured teeth with more than 50% enamel loss. 3. Patients with poor oral hygiene and lack of motivation. 4. Pregnant women. 5. Patients with abnormal occlusion (eg. edge to edge, deep bite, …) 6. Patients with parafunctional habits (eg. Bruxism, biting on hard objects, …) 7. Patients with endodontically treated teeth. 8. Lack of opposite occluding dentition in the area intended for restoration. 9. Psychiatric problems or unrealistic expectations. |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| n/a | |||
| Lead Sponsor | Collaborator |
|---|---|
| Marwa Salem |
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| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Retention of laminate veneers | using USPHS criteria for clinical evaluation | 1 year | No |
| Primary | Fracture of laminate veneers | using USPHS criteria for clinical evaluation | 1 year | No |
| Primary | Marginal adaptation of laminate veneers | using USPHS criteria for clinical evaluation | 1 year | No |