K05.3 K02.9
Conditions
Interventions
Group 1: First examination is perfomed simultanously with inclusion in the study. The volunteers are clinically examined after 1 and 2 weeks. After this baseline, the diet will be changed to a diet wi
Sponsors
Klinik für Zahnerhaltungskunde & Parodontologie, Universitätsklinikum Freiburg
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: written consent good general health gingivitis (GI >1) basic nutrition other than study-aimed nutrition
Exclusion criteria
Exclusion criteria: severe general diseases (HIV, Hepatitis B and C, acute tumor diseases), gravidity and breast feeding, intake of antibiotics within the last 6 months, participation in other studies, now or within the past 30 days , antiinflammatory drug intake like cortison, aspirin, interferon alpha, diabetes type I and II, intolerance of special nutrition like fruits, protein, gluten, severe chronic periodontitis, diseases influencing the production of saliva , smokers (>5 cig/d)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of Bleeding on Probing, comparing baseline with the last examination (after 6 weeks intervenion / 8 weeks after baseline). | — |
Secondary
| Measure | Time frame |
|---|---|
| Compliance of change in diet (evaluation of diaries) | — |
Countries
Germany
Contacts
Public ContactChristian Tennert
Universitätsklinikum Freiburg, Department fur Zahn-, Mund- und Kieferheilkunde, Klinik für Zahnerhaltungskunde und Parodontologie
Outcome results
None listed