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N/A Completed N=72 Randomized Triple-blind Treatment

Esthetics of Dental Composite and Adhesive System

Cavities of Teeth
Source: ClinicalTrials.gov NCT03716349 ↗
Enrolled (actual)
72
Serious AEs
0.0%
Results posted
May 2026
Primary outcomePrimary: Patient Satisfaction of the Restoration's Appearance (Esthetics) Using the Visual Analog Scale — 85; 79 units on a scale

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.

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

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. Informational only — not medical advice.

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