on-surgical treatment of peri-implantitis.
- Conditions
- Peri-implantitis
- Registration Number
- NL-OMON26244
- Lead Sponsor
- Dr. Marja LaineSection Periodontology, ACTAGustav Mahlerlaan 30041081 LA Amsterdam020-598 0 498
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 48
Inclusion Criteria
1. Dentate or edentate patients with at least one screw-type titanium implant;
2. The implant should be in function for at least a period of 12 months;
Exclusion Criteria
1. Patient with a history of taking systemic antibiotics in the preceding 3 months;
2. Patient allergic to penicillin (amoxicillin) or metronidazole;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method In periodontal literature a general consensus is used for clinical attachment level (CAL). A difference of 1 mm between treatments for CAL changes at initially deep pockets would be clinically relevant.
- Secondary Outcome Measures
Name Time Method In periodontal literature a general consensus is used for pocket probing depth (PPD). A difference of 1 mm between treatments for PPD changes<br>at initially deep pockets would be clinically relevant. Bone loss should be stabilized and not show any further loss on the radiographs. Plaqueaccumulation and bleeding on probing reduction by a minimum of 50%.<br /><br>The end point for microbiological parameters are less anaerobic bacteria and a shift in composition.