Evaluating Universal Adhesives in Cervical Lesions

NCT07459374 · tracked via the Priya Life Science Turkey tracker

Sponsor

Hacettepe University

Phase

Not applicable

Started

2024-03-19

Last updated

2026-03-09

Condition(s) studied

Cervical LesionDental

Investigational drug(s) / intervention(s)

G2 Bond Universal, GC Europe N.V., Leuven, BelgiumScotchbond Universal Plus, 3M ESPE, St. Paul, MN, USATokuyama Universal Bond II, Tokuyama Dental, Tokyo, Japan

G2 Bond Universal, GC Europe N.V., Leuven, Belgium: G2 Bond Universal, GC Europe N.V., Leuven, Belgium

Scotchbond Universal Plus, 3M ESPE, St. Paul, MN, USA: Scotchbond Universal Plus, 3M ESPE, St. Paul, MN, USA

Tokuyama Universal Bond II, Tokuyama Dental, Tokyo, Japan: Tokuyama Universal Bond II, Tokuyama Dental, Tokyo, Japan

Study 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.

Eligibility

Sex

ALL

Min age

18 Years

Max age

55 Years

Healthy volunteers

Accepted

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

Primary outcome measure(s)

Restoration survival rate at 12 months — From baseline to 12 month
Restoration survival rate at 12 months, defined as: At least 90% of restorations remaining in situ No statistically significant difference among groups according to FDI criteria

Trial sites (1)

Facility	City	Region	Status
Hacettepe University	Ankara	Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07459374 on ClinicalTrials.gov ↗ ← All trials in Turkey