Evaluation of resin with antimicrobial
Not Applicable
- Conditions
- Biofilmgingivitisperiodontal diseasebacteries infectious.C07.465.714.258.480G06.120C07.465.714
- Registration Number
- RBR-4tk434
- Lead Sponsor
- niversidade do Estado do Rio de Janeiro
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Data analysis completed
- Sex
- Not specified
- Target Recruitment
- Not specified
Inclusion Criteria
Male or female, aged between 18 to 32, healthy with no history or presence of a systemic disease, and absence of active caries or periodontal disease.
Exclusion Criteria
Individuals with removable prosthesis, orthodontic appliances or any dental implants; pregnant or breastfeeding; smokers; presence of cleft palate that precludes the wearing of a retainer; use of an antimicrobial mouthwash prior to enrolment in the study; and use of antibiotics against infectious diseases during the 3 months prior to the study.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Expected outcome 1: The reduction of biofilm formation on the surface of the acrylic resin in chlorhexidine is expected to be 50% compared to the control group after 24 hours in the buccal medium. The method used was by counting colonies on blood agar medium and Streptococcus mutans.;Conclusion1: There was no decrease in biofilm formation on the acrylic resin surface with chlorhexidine compared to the control group after 24 hours in the buccal medium. The method used was by counting colonies on blood agar medium and Streptococcus mutans.
- Secondary Outcome Measures
Name Time Method Secondary outcomes are not expected