Clinical Trials Directory

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

TypeNameDescription
OTHERSurefil 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.
OTHERFiltek OneScotchbond™ 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.