Trials / Completed
CompletedNCT06120868
Comparative Clinical Evaluation Between a Novel Self Adhesive and Conventional Bulk-fill Composites
Comparative Clinical Evaluation Between a Novel Self Adhesive and Conventional Bulk-fill Composites (a Randomized Controlled Clinical Study)
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Nourhan M.Aly · Academic / Other
- Sex
- All
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
This study aimed to evaluate the clinical performance of a novel, tooth-colored, self-adhesive bulk-fill restorative, and a conventional bulk-fill composite, for restoring class II cavities.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Surefil one® | For Surefil one® restorations, the capsule will be activated by pressing it against a stable surface, then mixed in a capsule mixer for 10 s. The capsule tip will be inserted into the proximal box, and the material is extruded as the tip is gradually moved in a coronal direction, ensuring that the material adapts to the cavity bottom and walls. |
| OTHER | Filtek One | Scotchbond™ Universal (SBU) will be used as an adhesive system in self-etch mode for FiltekTM One restoration. SBU will be applied actively for 20 seconds with a disposable brush tip, air-dried gently for 5 seconds to create a consistent bond thickness, then light-cured for 10 seconds. The FiltekTM One will be packed in increments up to 4 mm thick. A second layer of FiltekTM One will be applied on top of the first 4-mm layer if 4 mm is not adequate to properly restore the tooth. Each increment will be light cured for 20 seconds. |
Timeline
- Start date
- 2022-07-10
- Primary completion
- 2023-09-01
- Completion
- 2023-09-01
- First posted
- 2023-11-07
- Last updated
- 2023-11-07
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT06120868. Inclusion in this directory is not an endorsement.