N/A
N=28
Adhese One F Upgrade in Direct Filling Therapy
Dental Adhesive
Bottom Line
View on ClinicalTrials.gov: NCT02175368 ↗Enrolled (actual)
28
Serious AEs
0.0%
Results posted
Apr 2018
Primary outcome: Primary: Number of Participants With Clinical Success — 28 Participants
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Adhese One F Upgrade (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Ivoclar Vivadent AG
- Primary completion
- Jun 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Participants With Clinical Success |
28 | — |
| SECONDARY Clinical Quality |
28; 0 | — |
Summary
Investigation on the clinical performance of a new dental adhesive when used in direct filling therapy after phosphoric acid etching.
Hypothesis: The new adhesive shows an acceptable clinical performance and allows a good filling quality.
Eligibility Criteria
Inclusion Criteria
- indication for class I or II filling
- max. 2 restorations per patient
- vital teeth
- sufficient language skills
Exclusion Criteria
- dry working field cannot be established
- if the patient is known to be allergic to any of the materials' ingredients
- severe systemic diseases
- pregnancy
- non-vital or pulpitic teeth
- indication for indirect restoration
Data sourced from ClinicalTrials.gov (NCT02175368). 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.