Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities
Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities - A Randomized Controlled Clinical Trial
Misr International University
54 participants
Mar 14, 2023
INTERVENTIONAL
Conditions
Summary
The aim of this randomized clinical trial is to compare the six months clinical performance of the self-adhesive bulk-fill composite with the conventional nano-hybrid composite in the cervical lesions of teeth in the esthetic zone. In addition, to evaluate patient's satisfaction towards the self-adhesive bulk-fill material and its total operatory time.
Eligibility
Inclusion Criteria7
- Cervical lesions.
- Cervical lesions of at least one mm depth; to include enamel and dentin.
- Cervical lesions of not more than 3 mm in depth.
- Male or female genders.
- Medically free patients.
- Normal occlusion.
- Healthy Gingiva
Exclusion Criteria10
- Teeth showing signs of pulpitis or periapical pathosis.
- Patients older than 60 years.
- Patients younger than 18 years old.
- Pregnant women.
- Patients with history of allergy to resin.
- Patients with disabilities.
- Carious cervical lesions extending to proximal surfaces.
- Carious cervical lesions on the palatal/lingual surfaces.
- Teeth with root caries.
- Endodontically treated teeth.
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Interventions
It is a new self-adhesive bulkfill composite that requires no previous adhesive steps.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06394440