L43.8
Conditions
Interventions
Group 1: Patients and Study Participants
The study examines 20 patients with OLP (oral lichen planus), all of whom are being treated at the Department of Dermatology and Allergology at the University
these individuals are recruited from the recall program of the Department of Prosthodontics.
Clinical Examination
A current medical history is obtained prior to each examination. Furthermore, followi
correlation coefficients greater than 0.8 are considered acceptable. If values ??fall below this threshold, the examiners undergo further training to standardize the clinical examination procedure.
U
Sponsors
Med. Zentrum fu¨r Zahn-, Mund- und Kieferkrankheiten Klinik fu¨r Zahna¨rztliche Prothetik Phillips-Universita¨t Marburg Universita¨tsklinikum Gießen und Marburg GmbH,
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - Diagnosis of OLP in the patients - No diagnosis of OLP or other oral mucosal diseases in the study subjects
Exclusion criteria
Exclusion criteria: Age under 18 at the time of examination
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between the sonographically measured width of rete pegs and epithelial thickness, and the presence of oral lichen planus. | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation between sonographically recorded echogenicity and soft tissue perfusion and the presence of oral lichen planus. | — |
Countries
Germany
Contacts
Public ContactReiner Mengel
Med. Zentrum fu¨r Zahn-, Mund- und Kieferheilkunde Klinik fu¨r Zahna¨rztliche Prothetik
Outcome results
None listed