The effect of Stannous Fluoride Toothpaste in the treatment of Experimental Peri-implant Mucositis and Gingivitis: a randomized, double-blind, parallel-arm clinical trial
- Conditions
- Peri-Implantitis
- Registration Number
- RBR-4hq4kd8
- Lead Sponsor
- Faculdade de Odontologia da Universidade de São Paulo (FOUSP)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
Volunteers with a minimum age of 18 years; with implant-supported single-unit screw-retained crown in the molar or premolar region with more than one year in function; with one molar or premolar tooth in the same arch as the implant; with a minimum of 20 teeth in function; periodontally healthy; with absence of infection, radiographic bone loss, and probing depth less than 4 mm at periodontal sites or less than or equal to 5 mm at peri-implant sites; with presence of at least 2 mm of peri-implant keratinized tissue; with full-mouth bleeding scores and full-mouth plaque scores less than or equal to 20%
Volunteers using antibiotics in the last 3 months; with implant insertion depth more than or equal to 3 mm; with diseases or systemic conditions that require the use of systemic anti-inflammatory drugs, antibiotics, anticoagulants, and others; smokers; diabetics; with an allergy to toothpaste or mouthwashes; pregnant or breastfeeding women
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method