Active — Not RecruitingNot Applicable

Evaluating Universal Adhesives in Cervical Lesions

Turkey (Türkiye)30 participantsStarted 2024-03-19

Plain-language summary

The aim of this randomized controlled clinical trial is to evaluate the 12-month clinical performance of restorations placed in NCCLs using universal adhesives with different compositions according to FDI criteria.

Who can participate

Age range18 Years – 55 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: * Healthy individuals aged 18-55 years * No systemic condition contraindicating restorative treatment * Brushing teeth at least twice daily * At least 20 teeth in occlusion * At least three vital posterior teeth with non-carious cervical lesions and antagonist teeth * Completed initial periodontal therapy * Signed informed consent Exclusion Criteria: * Healthy individuals aged 18-55 years * No systemic condition contraindicating restorative treatment * Brushing teeth at least twice daily * At least 20 teeth in occlusion * At least three vital posterior teeth with non-carious cervical lesions and antagonist teeth * Completed initial periodontal therapy * Signed informed consent

What they're measuring

Restoration survival rate at 12 months

Timeframe: From baseline to 12 month

Trial details

NCT IDNCT07459374

SponsorHacettepe University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-03-19

View on ClinicalTrials.gov More Cervical Lesion trials