K05.3
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Written informed consent Diagnosis of periodontitis (Stage I or Stage III/IV according to the current classification) Planned guideline-based periodontal treatment at the Department of Conservative Dentistry and Periodontology, University Hospital Cologne Willingness to participate in all scheduled study visits and follow-up examinations
Exclusion criteria
Exclusion criteria: Age <18 years No written informed consent No indication for periodontal treatment Inability to understand the study or provide informed consent Pregnancy or breastfeeding (due to the study-related blood sampling) Acute systemic infections or other medical conditions that, in the opinion of the investigators, may interfere with study participation or interpretation of the results
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome: Change in interleukin-6 (IL-6) concentrations in gingival crevicular fluid (GCF) and EDTA plasma between baseline and follow-up visits (AIT, BEV, UPT). Assessment: Baseline, AIT, BEV and UPT. Assessment method: Quantification using a bead-based multiplex immunoassay (Luminex/NULISA or equivalent multiplex platform). | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes: Changes in local and systemic inflammatory and SASP markers. Characterization of local cellular senescence markers (cell-cycle arrest and DNA damage response) in gingival/granulation tissue. Changes in the composition of the supra- and subgingival microbiome. Changes in clinical periodontal parameters (PPD, CAL, BoP, plaque index). Association between age, immunosenescence and response to periodontal therapy. | — |
Countries
Germany
Contacts
Universitätsklinikum Köln Poliklinik für Zahnerhaltung und Parodontologie