Clinical Trials Directory

Trials / Unknown

UnknownNCT04854655

Evaluation of Ion Releasing Hybrid Restorative Material

Evaluation of Calcium and Phosphate Releasing Hybrid Restorative Material and Fluoride Releasing Hybrid Restorative Material Versus the Conventional Resin Composite in Proximal Carious Lesions Over One Year Follow-up Using USPHS Criteria

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
45 (estimated)
Sponsor
Cairo University · Academic / Other
Sex
All
Age
25 Years – 40 Years
Healthy volunteers
Accepted

Summary

Esthetic and mechanical evaluation of calcium and phosphate releasing hybrid restorative material and fluoride releasing hybrid restorative material versus the conventional nanofilled resin composite in proximal carious lesions over 1 year follow-up according to the USPHS criteria.

Detailed description

3 groups of 45 patients will receive class II restorations by using calcium and phosphate releasing hybrid restorative material (Activa Presto), fluoride releasing hybrid restorative material (Giomer), and conventional nanofilled resin composite. Then these restorations evaluated at 24 hours after placement, 1 month, 3 months, 6 months and 12 months according the modified USPHS criteria in terms of fracture, marginal adaptation, retention, anatomic form, marginal discoloration, surface texture, and color match.

Conditions

Interventions

TypeNameDescription
OTHERConventional resin compositenanofilled resin composite
OTHERActiva Prestocalcium and phosphate hybrid material
OTHERGiomerfluoride releasing hybrid material

Timeline

Start date
2021-10-10
Primary completion
2022-10-10
Completion
2022-10-30
First posted
2021-04-22
Last updated
2021-09-09

Source: ClinicalTrials.gov record NCT04854655. Inclusion in this directory is not an endorsement.