Clinical Evaluation of Esthetic Restorations Placed in Primary Molars With Composite Resin Enriched With Insoluble Anti Bacterial Nano Particles (IABN)
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|ClinicalTrials.gov Identifier: NCT00389714|
Recruitment Status : Unknown
Verified December 2007 by Hadassah Medical Organization.
Recruitment status was: Not yet recruiting
First Posted : October 19, 2006
Last Update Posted : December 11, 2007
Composite resins are presently among the most popular esthetic restorative materials in dentistry. These materials offer excellent esthetic appearance, allow for conservative cavity preparation and are now becoming widely accepted for clinical use in primary molars 1-23. Despite the improvement of their properties, achieved with better materials and incremental placing techniques, composite resin restorations appear to have still several drawbacks: although similar to amalgam in short terms studies, they have a high long term failure rate, mainly due to discoloration, loss of retention and secondary caries3,11,19, are time-consuming and technique sensitive, lack anti-cariogenic potential and can be amenable to secondary caries at the cervical dentin margins 1, 2.
Continued interest in providing advance in restorative esthetic materials led to the development of new generations of composites. Among the newest material developed is the use of minute amount of nanoparticles which convert composites to possess permanent antibacterial properties.
It is of great interest to observe the clinical behavior of this new material when utilized in clinical practice. Thus the aims of the present in-vivo study are:
- To evaluate the clinical and radiographic performance of the New Restorative System when placed with adhesive systems in class II restorations of primary molars.
- To assess, by SEM, the micromorphology of the cervical, buccal and lingual margins of the proximal surfaces of the restored teeth retrieved after exfoliation or extraction.
- To asses, by means of polarized light microscopy, the integrity of the cervical margins of the same retrieved teeth.
|Condition or disease||Intervention/treatment||Phase|
|Dental Carious Dental Filling||Device: dental restoration||Phase 2|
Show Detailed Description
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||60 participants|
|Intervention Model:||Crossover Assignment|
|Official Title:||Phase 2 Clinical Study :Evaluation of the Efficacy of Insoluble Antibacterial Nanoparticles Incorporated Into Commercialy Used Composit Resins as an Esthetic Restoration Material in Children|
|Study Start Date :||February 2007|
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00389714
|Contact: Michael Perez Davidi, DMD||+972 54 email@example.com|
|Hadassah Medical Organization||Not yet recruiting|
|Jerusalem, Israel, 46540|
|Contact: Arik Zukhert, DMD 00 972 2 6776095 firstname.lastname@example.org|
|Contact: Hadas Lemberg, PhD +972543113780 email@example.com|
|Principal Investigator: Michael Perez Davidi, DMD|
|Study Director:||Michael Perez Davidi, DMD||Hadassah Medical Organization|
|Study Chair:||Ana Fux, DMD||Hadassah Medical Organization|
|Study Director:||Mordechay Moskovitch, DMD||Hadssah Medical Orgenization|