Monitoring of Non-Surgical Treatment of Peri-implantitis, Traditional Measurement Methods and aMMP-8 Test Technology-Cross Sectional Study
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Peri-implant Mucositis
- Sponsor
- Lahanna oy
- Enrollment
- 40
- Locations
- 1
- Primary Endpoint
- the result of the participants who were measured aMMP-8
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
This study aimed to investigate the response to non-surgical treatment of peri-implantitis diseases during the maintenance phase. The patients underwent non-surgical implant maintenance treatment, and the success of the treatment was measured again after 30 days using the same criteria and methods.
Detailed Description
For 40 patients, the aMMP-8 test was performed on the buccal gingival pocket of the implant teeth, gingival bleeding (BOP), implant pocket depth (PPD), and a periapical x-ray to measure radiologic bone level (RBL) were taken.
Investigators
Eligibility Criteria
Inclusion Criteria
- •implant patients arriving for a maintenance visit at a dental clinic
- •a diagnosis of peri-implant healthy, peri-implant mucositis, or peri-implantitis by a dentist
- •a written informed consent.
- •Exclusion Criteria
- •age under 25
- •antibiotic treatment within six months
- •the maintenance treatment had been completed within 6 months.
Exclusion Criteria
- Not provided
Outcomes
Primary Outcomes
the result of the participants who were measured aMMP-8
Time Frame: 1 month
Measure aMMP-8-level ng/ml
the result of the participants who were measured BOP
Time Frame: 1 month
measure bleeding on probing in PISF
the result of the participants who were measured PPD
Time Frame: 1 month
measure peri-implant pocket depth