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Evaluating Universal Adhesives in Cervical Lesions

NCT07459374 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-03-09

No results posted yet for this 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.

Conditions

  • Cervical Lesion
  • Dental

Interventions

DEVICE

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

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

DEVICE

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

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

DEVICE

Tokuyama Universal Bond II, Tokuyama Dental, Tokyo, Japan

Tokuyama Universal Bond II, Tokuyama Dental, Tokyo, Japan

Sponsors & Collaborators

  • Hacettepe University

    lead OTHER

Principal Investigators

  • Cansu Atalay, Assoc. Prof. · Hacettepe University

  • Aybüke Uslu Tekce, Assist. Prof. · Hacettepe University

  • Ayşe Rüya Yazıcı, Prof. · Hacettepe University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-03-19
Primary Completion
2025-03-19
Completion
2028-03-19

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07459374 on ClinicalTrials.gov