Trials / Completed
CompletedNCT03556553
Clinical Evaluation of a Self-Adhering Flowable Composite in Class I Cavities
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 25 (actual)
- Sponsor
- Hacettepe University · Academic / Other
- Sex
- All
- Age
- 16 Years – 65 Years
- Healthy volunteers
- Accepted
Summary
The aim of this study is to evaluate long-term clinical performance of a self-adhering flowable resin composite in comparison with a conventional flowable resin composite used with an etch\&rinse adhesive system in minimally invasive class I cavities. Twenty-five patients will receive at least one pair of class I restorations. After class I cavities were prepared they were restored either with a self-adhering flowable resin composite (VertiseFlow/Kerr-VR) or with a flowable resin composite (Luxaflow/DMG-LX) in combination with an etch\&rinse adhesive (Teco/DMG) \[according to the manufacturers' instructions. Restorations will be evaluated at baseline and yearly according to FDI criteria by two evaluaters. Statistical analysis will be carried out with Pearson Chi-Square test and Cochran Q-test followed by Mc Nemar's.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Vertise Flow | Composite resin |
| DEVICE | LuxaFlow | Composite resin |
| DEVICE | Teco Adhesive | Adhesive system |
Timeline
- Start date
- 2011-03-30
- Primary completion
- 2011-06-30
- Completion
- 2016-06-30
- First posted
- 2018-06-14
- Last updated
- 2021-09-14
Source: ClinicalTrials.gov record NCT03556553. Inclusion in this directory is not an endorsement.