Evaluation of Cervical Restorations Performance Using Modified Universal Adhesive (NCT05509127) | Clinical Trial Compass
Active — Not RecruitingPhase 1
Evaluation of Cervical Restorations Performance Using Modified Universal Adhesive
Egypt50 participantsStarted 2023-01-01
Plain-language summary
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.
Who can participate
Age range20 Years – 40 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:
* 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.