CompletedNot Applicable

HEMA-free Universal Adhesives for Restoring Non-carious Cervical Lesions

Egypt28 participantsStarted 2023-01-15

Plain-language summary

because of the recent introduction of universal adhesives, little information is currently available about the bond durability of universal adhesives to various substrates. Evaluation of bond durability is important since the stability of the bond between the adhesive and substrates is related to the clinical success of restorations. Because significant hydrolysis of the dentin-resin interface occurs after 6-12 months, a clinical trial of at least 18 months' duration is indicated to more accurately depict the likelihood of long-term clinical success

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: * Participants had to be in good general health, be at least 18 years old * have an acceptable oral hygiene level * Participants were required to have NCCLs in different teeth preferably anterior or posterior that needed to be restored. * These lesions had to be noncarious * deeper than 1 mm * involve both the enamel and dentin of vital teeth without mobility. Exclusion Criteria: * Uncooperative behavior, limits the use of adhesive due to hampering of adequate field or isolation techniques throughout the procedure. * Patients allergic to the adhesive material. Patients with extremely poor oral hygiene * severe or chronic periodontitis * heavy bruxism habits * Pulp involvement

What they're measuring

Primary outcome (marginal staining)

Timeframe: 18 months

Trial details

NCT IDNCT05497583

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2024-09-20

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