K00.9
Conditions
Interventions
Group 1: one-off fluoride varnish application + staggered time points of sensitivity measurement
Group 2: two fluoride varnish application with an interval of one week + uniformly graduated sensitivit
Sponsors
Universitätsklinikum Jena
Eligibility
Sex/Gender
All
Age
6 Years to 17 Years
Inclusion criteria
Inclusion criteria: children ( aged 6-17) with MIH Children and adolescents with MIH (for recording disease perception) Children and adolescents with MIH and hypersensitivity (for testing of pain reduction by fluoride lacquer application)
Exclusion criteria
Exclusion criteria: -the presence of diseases or disabilities that do not allow an assessment of sensitivity -presence of intolerance to components of the fluoride varnish -ulcerative gingivitis or ulcerative -oral mucosal disorders -no consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Proof of whether and for what period of time a pain reduction of hypersensitive MIH teeth is achieved by a single application of a commercially available fluoride varnish (Profluoride Varnish, VOCO, Cuxhaven) 2. Demonstration of whether a second application of the same fluoride varnish after one week of single application is superior in reducing hypersensitivity. | — |
Secondary
| Measure | Time frame |
|---|---|
| Assessment of the perception of MIH in children affected by MIH using the adapted Illness Perception Questionnaire/Dental [Nelson et al. , 2016] | — |
Countries
Germany
Contacts
Public ContactIna Schüler
Universitätsklinikum Jena
Outcome results
None listed