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.
Age range
19 Years – 90 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
FDI 11 - Postoperative Hypersensitivity
Timeframe: Baseline
Pulp Integrity
Timeframe: Baseline
Overall Survival Rate
Timeframe: Baseline
FDI 11 - Postoperative Hypersensitivity
Timeframe: 6 Month
Pulp Integrity
Timeframe: 6 Month
Overall Survival Rate
Timeframe: 6 Month
FDI 11 - Postoperative Hypersensitivity
Timeframe: 12 Month
Pulp Integrity
Timeframe: 12 Month
Overall Survival Rate
Timeframe: 12 Month
FDI 11 - Postoperative Hypersensitivity
Timeframe: 24 Month
Pulp Integrity
Timeframe: 24 Month
Overall Survival Rate
Timeframe: 24 Month
FDI 11 - Postoperative Hypersensitivity
Timeframe: 36 Month
Pulp Integrity
Timeframe: 36 Month
Overall Survival Rate
Timeframe: 36 Month