Actively Recruiting
Long-term Surgical Treatment Outcome of Peri-implantitis Lesions
Led by Malmö University · Updated on 2024-02-16
650
Participants Needed
3
Research Sites
539 weeks
Total Duration
On this page
Sponsors
M
Malmö University
Lead Sponsor
M
Medical University of Vienna
Collaborating Sponsor
AI-Summary
What this Trial Is About
The surgical treatment outcome of patients that have been or are consecutively treated at the University of Malmö, at Blekinge hospital, and at the Dental Clinic of the Sigmund Freud University Vienna will be evaluated on an a regular base; specifically all patients treated since 2014 and those receiving treatment in the future, will be regularly assessed, max. once per year after the 1-year control from the surgical intervention for clinical and radiographic assessment of healing. Clinical peri-implant parameters (e.g., probing pocket depth) and peri-implant sulcus fluid (PISF) are collected, and a peri-apical radiographic examination is made. Further, from 200 patients treated in the future, the inflammatory peri-implant lesion will be collected and subjected to histological, microbiological, and molecular analysis. The removal of these lesions is a standard procedure and performed in all patients independent of study participation; i.e., the lesion has anyway to be removed during surgery and if the lesions are not stored, they would be thrown.
CONDITIONS
Official Title
Long-term Surgical Treatment Outcome of Peri-implantitis Lesions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients treated since 2014 or those continuously being treated
- Patients called for regular annual check-ups after surgical intervention
- Patients willing to undergo clinical and radiographic assessments annually
You will not qualify if you...
- Implant loss
AI-Screening
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Trial Site Locations
Total: 3 locations
1
Dental Clinic, Sigmund Freud University Vienna
Vienna, Austria
Actively Recruiting
2
Blekinge hospital
Karlskrona, Sweden
Actively Recruiting
3
Malmö University
Malmö, Sweden
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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