RecruitingNot Applicable

Clinical Evaluation of Self-Adhesive Bulk-Fill Composite Versus Conventional Nano-hybrid Composite in Cervical Cavities

Egypt54 participantsStarted 2023-03-14

Plain-language 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.

Who can participate

Age range18 Years – 60 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: * 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 Criteria: * 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.

What they're measuring

Clinical efficacy of the self-adhesive bulkfil composite in comparison to conventional composite

Timeframe: Six months

Trial details

NCT IDNCT06394440

SponsorMisr International University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-07-20

View on ClinicalTrials.gov More Cervical Caries trials