Clinical Performance Clinical Trial
Official title:
Evaluation of Cervical Restorations Performance Using Modified Universal Adhesive Compared to Conventional Universal Adhesive: A Randomized Clinical Trial
Verified date | November 2022 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Class V restorations are evaluated to reveal whether the use of modified universal adhesive will have a similar performance compared to conventional universal adhesive or not.
Status | Not yet recruiting |
Enrollment | 30 |
Est. completion date | December 2024 |
Est. primary completion date | June 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years to 40 Years |
Eligibility | Inclusion Criteria: - Small to moderate carious cervical lesions. (ICDAS scores 3,4) - Upper premolar teeth. - Good oral hygiene (mild to moderate plaque accumulation) - Vital teeth with no signs of irreversible pulpitis. - Presence of favorable occlusion and normal contact with adjacent teeth. Exclusion Criteria: - Patients with systemic diseases, severe medical complications or allergic history concerning methacrylates. - Lack of patient compliance, pregnancy, rampant caries, heavy smoking or xerostomia. - Evidence of parafunctional habits and TMJ disorders. - Class V lesions in molars. - Non-carious cervical lesions. - Deep carious defects (close to pulp, less than 1 mm distance). - Teeth with signs and symptoms of irreversible pulpitis or pulp necrosis. - Endodontically treated teeth. - Tooth hypersensitivity. - Possible prosthodontic restoration of teeth. - Heavy occlusion and occlusal contacts or history of bruxism. - Severe periodontal affection. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Marginal adaptation | using Modified USPHS criteria | Baseline, 6 months, 12 months and 18 months. | |
Secondary | Marginal discoloration | using Modified USPHS criteria | Baseline, 6 months, 12 months and 18 months. | |
Secondary | Post-operative sensitivity | using Modified USPHS criteria | Baseline, 6 months, 12 months and 18 months. | |
Secondary | Retention | using Modified USPHS criteria | Baseline, 6 months, 12 months and 18 months. | |
Secondary | Secondary caries | using Modified USPHS criteria | Baseline, 6 months, 12 months and 18 months. |
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