Apical access for treatment of peri-implantitis
Not Applicable
- Conditions
- Advanced peri-implantitisOral Health
- Registration Number
- ISRCTN16923588
- Lead Sponsor
- Arrow Development S.L.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
1. Aged = 18 years old
2. Peri-implant bone defect = 3mm assessed radiographically
3. PPD = 5mm combined with bleeding on probing or suppuration
4. Intra-surgically, the bone defect must have at least an intraosseous component of 3mm and a width of no more than 4mm implants = 1 year in function
Exclusion Criteria
1. Treated for peri-implantitis during the previous 6 months
2. Intake of systemic or local antibiotics during the previous 6 months
3. Pregnant patients
4. Systemically unhealthy patients
5. Patients allergic to collagen
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Treatment success will be defined as the absence of bleeding on probing (BoP)/pus, probing pocket depth (PPD) =5 mm and =1 mm recession measured using a periodontal manual probe CP 15 Hu-Friedy at 4, 12, 24 and 48 weeks after surgical therapy
- Secondary Outcome Measures
Name Time Method