At a glance
ClinicalIndex Comparison RecordN/ACompleted· 39 enrolled
Drug / intervention
Tetric PowerFilldevice
Likely dose
Tetric PowerFill bulk fill resin composite applied to posterior teeth via PowerCure systemAI-extracted
Key inclusion· 7
- ✓At least 1 restoration needed in a vital posterior tooth
- ✓Restoration width ≥1/3 distance from buccal to lingual cusp tips
- ✓Restored teeth must have occlusal contact with opposing teeth
- ✓Minimum 75% Class II restorations and 25% Class I
Key exclusion· 9
- ✕Allergy to composite resin monomers or other materials being investigated
- ✕Severe medical complications (organ transplants, long-term antibiotics/steroids, cancer, immunocompromised)
- ✕Xerostomia from medications, radiation, or Sjögren's syndrome
- ✕Advanced or severe periodontitis, rampant caries, or poor oral hygiene
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Clinical Evaluation of a Bulk Fill Resin Composite
In Brief
A clinical study evaluating Tetric PowerFill for Dental Caries and Unsatisfactory or Defective Restoration of Tooth. Completed, enrolled 39 participants across 1 site.
Detailed Summary
The purpose of this clinical trial is to measure the clinical outcomes of Tetric PowerFill Class I and II restorations cured in 3 seconds with the Bluephase PowerCure curing unit.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
201820192020202120222023202420252026
Enrollment StartDec 2017
First PostedDec 2020
Primary CompletionJun 2021
TodayJul 2026
First PostedDec 28, 2020
Enrollment StartDec 1, 2017
Primary CompletionJun 30, 2021
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 5.5 years ago
Interventions
Tetric PowerFilldevice
Tooth (teeth) affected by dental caries or with an existing defective filling will be restored using the PowerCure system.