To Access the Effects of Mucositis in Adults With Dental Implants
- Registration Number
- NCT01072201
- Lead Sponsor
- Colgate Palmolive
- Brief Summary
Clinical research for the treatment of mucositis subjects who have dental implants for a minimum of one-year.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 60
- Male and female subjects, ages 30-70.
- Availability for the six-month duration of the clinical research study.
- Good general health.
- Subjects who have lost teeth for periodontal disease reasons and who have been restored with implants.
- Minimum of 5 remaining teeth and a minimum of 2 implants.
- Initial evaluation of the gingival and peri-implant mucosal tissues by determining full mouth bleeding on probing.
- Initial plaque evaluation by determining full mouth presence/absence of plaque.
- Signed Informed Consent Form.
- Tumor(s) of the soft or hard tissues of the oral cavity.
- Untreated periodontal disease (purulent exudate, tooth mobility, and/or extensive loss or periodontal attachment or alveolar bone).
- Carious lesions requiring immediate restorative treatment.
- Uncontrolled Diabetes
- Use of antibiotics any time during the one month prior to entry into the study.
- Untreated peri-implantitis.
- Participation in any other clinical research study or test panel within the three months prior to entry into the study.
- Pregnant women or women who are breast feeding.
- History of allergies to personal care/consumer products or their ingredients.
- Medical condition which prohibits not eating/drinking for up to 2 hours.
- Current alcohol or drug abuse.
- Systemic or local disease conditions that would compromise post-operative healing.
- Regular use of anti-inflammatory drugs.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Total toothpaste Triclosan and Fluoride Triclosan/copolymer/fluoride toothpaste Ultrabrite toothpaste Fluoride Fluoride Toothpaste
- Primary Outcome Measures
Name Time Method Bleeding on Probing 6 months Percentage of Bleeding Scale: The bleeding sites are identified by either a 0 or 1. (0=no bleeding \& 1= bleeding) The number of spots between teeth that bleed are divided by number of spots between teeth that are scored.
Mean Pocket Depth 6 Months Measurement scale: 0 millimeter measurement= no pocket depth. 3, 4, 5, \& 6 millimeter are indications of deeper Pocket depth.
Mean Percentage of Plaque Scores 6 Months Mean Percentage (%) of dental plaque on all tooth surfaces, including implants and natural teeth. Plaque Scale is 0=no plaque and 1= dental plaque present. Percentage is derived from sum of all plaque scores divided by the number of tooth surfaces scored.
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Ariminum Research & Dental Education Center
🇮🇹Rimini, Italy