Active — Not RecruitingNot Applicable

Clinical Evaluation of Composite Restorations Using Two-steps Universal Adhesive in Non-carious Cervical Lesion (NCCL)

Thailand55 participantsStarted 2023-11-10

Plain-language summary

The goal of this clinical study is to compare the clinical performance of a new 2-steps universal adhesive in patients with non-carious cervical lesions. The main question it aims to answer is: Is there any difference in clinical performance of a new 2-steps universal adhesives bonded with different etching strategies. Participants will have restorations using a new 2-steps universal adhesives in different etching strategies. * etch-and-rinse * selective enamel etching * self-etch

Who can participate

Age range18 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: * Available for follow-up visits * Have at least 28 teeth/ 20 teeth under occlusion * Have at least 3 non-carious cervical lesions without peri-apical lesion. The lesion is not nearly exposed pulp and no history of previous restoration. Exclusion Criteria: * Rampant / uncontrolled caries * Advanced untreated periodontal disease * \>2 cigarette packs/day * Systemic or local disorders that could not undergo dental procedures * Xerostomia * Severe bruxism, clenching, TMD * Pregnancy at the time of screening * Known history of sensitivity to resin or related materials * Fixed orthodontic appliance or planning to have orthodontic treatment within 3 years

What they're measuring

sensitivity (modified USPHS)

Timeframe: 3 years

retention (modified USPHS)

Timeframe: 3 years

secondary caries (modified USPHS)

Timeframe: 3 years

Trial details

NCT IDNCT05573243

SponsorMahidol University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-11

View on ClinicalTrials.gov More Non-carious Cervical Lesion trials