Nanosilver Fluoride to Prevent Dental Biofilms Growth (NSFCT)
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|ClinicalTrials.gov Identifier: NCT01950546|
Recruitment Status : Completed
First Posted : September 25, 2013
Last Update Posted : June 10, 2015
|Condition or disease||Intervention/treatment||Phase|
|Dental Caries||Drug: nanosilver fluoride||Phase 1|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||30 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||Double (Participant, Investigator)|
|Official Title:||Nanosilver Fluoride: a Microbiological and Clinical Trial|
|Study Start Date :||September 2014|
|Actual Primary Completion Date :||December 2014|
|Actual Study Completion Date :||January 2015|
Experimental: Nanosilver fluoride
This product is a solution composed of: 390 mg / ml 9nm silver nanoparticles ;21 mg / ml chitosan ; 22 mg / ml NaF.The cariostatic agent, nanosilver fluoride, was formulated in a similar way to silver diamine fluoride, so that this new formulation contained 5% nanosilver fluoride, while commercial diamine silver fluoride contains 30% silver fluoride. It will be applied once with a microbrush on tooth surfaces to check if it prevents the growth of S. mutans biofilms on dental surfaces.
Drug: nanosilver fluoride
The product will be applied in the volunteers in the morning, before the first class, in relative isolation, made with cotton rolls and Vaseline to protect the soft tissue. It will apply 30mg of the product with microbrush, previously standardized in a pilot study on cervical vestibular surfaces of incisors and canines healthy, on a total of 8 teeth, 4 upper and 4 lower. After a period of 7 days,the cervical dental biofilms will be collect, third on the buccal surfaces of incisors and / or canines upper and lower, with the aid of sterile spatulas.
Other Name: silver nanoparticles
- Initial biofilm collecting before applying the product and after nanosilver fluoride application. [ Time Frame: one week ]The initial dental biofilm collection will be conducted to count colony-forming units of S. mutans and then the product will be applied on these dental surfaces after the collect. After one week, a new collect will be performed and the colony-forming units of S. mutans will be counting to compare with the initial.
- Evaluation of effectiveness of nanosilver fluoride on bacterial growth in the dental biofilm [ Time Frame: two weeks ]Collection of dental biofilm will be performed after two weeks of product application and colony count will be performed in the laboratory.
- Collection of dental biofilm will after four weeks of product application. [ Time Frame: Four weeks ]Collection of dental biofilm will be performed after four weeks of product application and colony count will be performed in the laboratory.
- Collection of dental biofilm after eight weeks of product application [ Time Frame: Eight weeks ]Collection of dental biofilm will be performed after eight weeks of product application and will be compared with the initial score of S. mutans colony forming units.
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): NCT01950546
|Escola Municipal Anita Trigueiro do Valle|
|João Pessoa, Paraíba, Brazil, 58046020|
|Study Director:||Aronita Rosenblatt, PhD||UPE|