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N/A N=72 Randomized Triple-blind Treatment

Esthetics of Dental Composite and Adhesive System

Cavities of Teeth

Enrolled (actual)
72
Serious AEs
0.0%
Results posted
May 2026
Primary outcome: Primary: Patient Satisfaction of the Restoration's Appearance (Esthetics) Using the Visual Analog Scale — 85; 79 units on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Pulp vitality testing (Diagnostic_test); Photos (Other); local and/or topical anesthetic (Drug); rubber dam (Device); tooth surface cleaned (Other); enamel margins (Procedure); Adhesive Systems (Procedure); cavity preparation (Procedure); Shade selection using Easy Shade 5 (Other); Light Curing (Procedure); Contoured and polished (Procedure); Consent (Other); Health Questionnaire (Other); xray (Radiation); Release of medical information signed (Other); Oral Exam (Other); Teeth Assessment (Other); Clinical Assessment (Other); Tokuyama Universal Bond (Device); ScotchBond (Device)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Erica Teixeira
Primary completion
Nov 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Patient Satisfaction of the Restoration's Appearance (Esthetics) Using the Visual Analog Scale
85; 79
SECONDARY
Patient Satisfaction of the Restoration Appearance (Esthetics) Using the Verbal Rating Scale
3.54; 3.16

Summary

To compare a newly developed filling composite to a current filling composite system. Two restorations will be placed in each subject, one using system A and one using system B. The first system listed in the randomization pair will be placed on first tooth (#4-#13), and the second system on 2nd tooth (#4-#13). The same three researchers will be responsible for placement of all the restorations.

Eligibility Criteria

Inclusion Criteria

  • Sensible tooth -responds to cold or electric pulp testing (done at screening)
  • Patient 18years of age or old
  • Current radiograph available (done at screening as needed)
  • A pair of the same type of restorations needed in the anterior esthetic/facial region (tooth #4-#13).

Exclusion Criteria

  • Fewer than 20 teeth
  • Advanced untreated periodontal disease or recent periodontal surgery
  • Rampant uncontrolled caries activity
  • Bruxism or clenching and visible wear facets on the occlusal surface
  • Undergoing or in need of TMJ therapy
  • Known allergy to methacrylate-based materials or product ingredients
  • History of poor dental visit attendance
  • Not available for recall for at least 3 years
  • Fractured or visibly cracked tooth
  • Poor oral hygiene
  • Sensitive tooth or currently using desensitizing treatments, pastes or medicaments
  • Pregnant
  • Abutment teeth for prostheses
  • Teeth considered for restoration are non-vital, have had root canal therapy or been pulp capped
  • Teeth or supporting structures with any symptomatic pathology or extensive caries lesion
  • Individual supervised by PI or supervised by member of research team
  • Individual subordinate to the PI or subordinate to any member of the research team
  • Student or trainee under the direction of the PI or under the direction of a member of the research team
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03716349). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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