Clinical Trial Details
— Status: Not yet recruiting
Administrative data
NCT number |
NCT05509127 |
Other study ID # |
Modified Universal Adhesive |
Secondary ID |
|
Status |
Not yet recruiting |
Phase |
Phase 1
|
First received |
|
Last updated |
|
Start date |
January 2023 |
Est. completion date |
December 2024 |
Study information
Verified date |
November 2022 |
Source |
Cairo University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Class V restorations are evaluated to reveal whether the use of modified universal adhesive
will have a similar performance compared to conventional universal adhesive or not.
Description:
The innovative Scotchbond Universal Plus Adhesive offers all the benefits of its predecessor,
Single Bond Universal Adhesive as demonstrated by a 3M field evaluation comparing the
performance of the two products. These benefits include:
- Compatibility with all etching techniques - total-etch, self-etch, and selective enamel
etch.
- Usage with direct and indirect indications.
- Bonding to all dental surfaces without the need for separate primers or silanes
- Virtually no post-operative sensitivity.
The newly modified adhesive with its careful formulation offers:
- Radiopacity like dentin to reduce the risk of X-ray misdiagnosis and overtreatment.
- Ability to bond and seal caries-affected dentin to support minimally invasive
preparation guidelines and maximize preservation of natural tooth structure.
- Adhesion to all dental substrates and all direct and indirect materials, including glass
ceramics.
- Full dual- and self-cure compatibility without the need for an additional dual-cure
activator bottle.
- A BPA derivative-free formulation to alleviate concerns about BPA in dental materials
- A fully aligned system with RelyXâ„¢ Universal Resin Cement, offering excellent bond
strength for virtually all dual-cure resin cement indications.
As with any new material or technique, long-term clinical evaluations are needed to
demonstrate the value of universal bonding agents adequately. So, the aim of this study is to
evaluate the clinical performance of the modified universal adhesive, versus the conventional
universal adhesive, for restoring carious class V cavities over one year and a half.