Implantoplasty versus titanium rotary brushes in the surgical treatment of peri-implantitis: a randomized controlled clinical trial
Not Applicable
Recruiting
- Conditions
- Not Applicable
- Registration Number
- KCT0007900
- Lead Sponsor
- Yonsei University Health System, Dental Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
1.A person who voluntarily signs a clinical research agreement
2.Patients present with =1 implant diagnosed with peri-implantitis
3.Radiographically confirmed peri-implant bone loss >3 mm and probing depth >6 mm, bleeding and/or suppuration on probing
Exclusion Criteria
1.history of surgical treatment for peri-implantitis
2.untreated periodontitis
3.pregnancy
4.intake of drugs affecting periodontal tissues
5.diabetes mellitus, other uncontrolled systemic diseases
6.smoking > 10 cigarettes per day
7.other uncontrolled systemic disease
8.the need of antibiotic prophylaxis and intake of antibiotics within the previous 1 months
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Treatment success (Composite outcome: PD =5 mm, absence of BOP & no additional bone loss)
- Secondary Outcome Measures
Name Time Method Clinical measurements;Changes of hard and soft tissue contours (periapical radiographs);Changes of hard and soft tissue contours (intraoral scan); Microbiological analysis; Biomarkers of inflammation;Surgery time