K02 K03
Conditions
Interventions
Group 1: Candida Professional Protect toothpaste (33 ppm P11-4, 1450 ppm fluoride), 1cm string/per use (30s) +
Candida Professional Protect mouth fluid (7.5 ppm P11-4), 5ml/per use (30s)
in total 5x
Sponsors
Mibelle AG
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Age = 18 years and = 65 years Willing and able to understand and to follow the study procedures and instructions Willing to wear a dental appliance for 3 days Willing and able to attend the on-study visits Good oral hygiene throughout the study Written informed consent before participation in the study
Exclusion criteria
Exclusion criteria: Volunteer with an active periodontal disease or periodontal surgery < 1 year prior to study participation Volunteer with hypersensitive teeth or with any other (painful) oral pathology or defect Volunteer with an orthodontic appliance Volunteer undergoing a medical treatment Volunteer who is allergic to dental products Pregnant and lactating woman Concurrent participation in another clinical trial
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Endpoint: S5 (32h after study start); When: max. 24 after S5 Method: Acid protection by means of profilometrie | — |
Secondary
| Measure | Time frame |
|---|---|
| Endpoint: S5 (32h after study start); When: max. 24 after S5 Method: Evaluation of the duration of the protective effect by the Curolox technology by means of profilometrie | — |
Countries
Germany
Contacts
Public ContactAnahita Jablonski-Momeni
Philipps-Universität Marburg, Medizinisches Zentrum für ZMK, Abteilung für Kinderzahnheilkunde
Outcome results
None listed