Dental plaque (amount)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participation requires written informed consent following prior information about the objectives and procedures of the study.
Exclusion criteria
Exclusion criteria: Exclusion criteria include known hypersensitivity to plaque-disclosing agents, acute oral mucosal lesions, inability to provide informed consent, and pregnancy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Diagnostic performance of fluorescence-based plaque visualization for plaque detection (plaque present/absent) compared with conventional plaque disclosure (reference standard), expressed by sensitivity and specificity. | — |
Secondary
| Measure | Time frame |
|---|---|
| - Inter-rater agreement - Ordinal plaque assessment - Image assessment time - Subjective evaluation and preference for the imaging modalities by the raters | — |
Countries
Germany
Contacts
Klinik für Zahnerhaltung, Parodontologie und Präventive Zahnheilkunde, Uniklinik RWTH Aachen