Prophylaxis of gingivitis Reduction of bacteremia after tooth brushing and reduction of pro-inflammatory mediators
Conditions
Interventions
Group 1: Clinical trial, interventional study with a form of waiting-group design:
Testgroup will receive a demand orientated oral intensive prophylaxis.
1. step: professional toothcleaning and oral h
Sponsors
Universitätsklinikum KölnZMMKAbteilung für Zahnerhaltung und Parodontologie
Eligibility
Sex/Gender
All
Age
6 Years to 25 Years
Inclusion criteria
Inclusion criteria: - Patients with a known renal insufficiency (stage III-V and after transplantation) - Patients with chronic renal insufficieny at the age of 6 to 25 years. - Patients with a higher risk of gingivitis (GI > 0; PSI stage 0-2) - Patients, who did not take antibiotics for the last 2 weeks - Patients who agreed the consent form written and verbal - Patients who do not participate in a different clinical trial
Exclusion criteria
Exclusion criteria: - Patients who do not have suitable conditions for a dental treatment - Patients who regulary have to take antibiotics
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Free of Gingivitis, measured by papilla bleeding index | — |
Secondary
| Measure | Time frame |
|---|---|
| A reduction of pro-inflammatory Mediators and risk of bacteremia | — |
Countries
Germany
Contacts
Public ContactKarolin Höfer
Universitätsklinikum KölnZMMKAbteilung für Zahnerhaltung und Parodontologie
Outcome results
None listed