M00-M25 C00-C14 Q87
Conditions
Interventions
Group 1: patients before TMJ TJR (Temporomandibular Joint Total Joint Replacement).
measurements: sEMG, maximum voluntary bite force, pain threshold, quality of life
Group 2: patients following unilat
Sponsors
Rheinische Friedrich-Wilhelms Universität Bonn,ZZMK-Zahnärztliche Prothetik
Eligibility
Sex/Gender
All
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Indication for TMJ TJR (Temporomandibular Joint Total Joint Replacement). Oral and written consent.
Exclusion criteria
Exclusion criteria: lack of consent of the patient, anatomical contraindications for attachment of the testing equipment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The muscle activity of the temporal and masseter muscles (s-EMG), measurement of the maximum voluntary bite force, musculoskeletal pain and oral health-related quality of life will be measured before TMJ TJR (Temporomandibular Joint Total Joint Replacement) and at 3, 6 and 12 months post-operatively. Subsequently, the measurements are made annually. The effect of the insertion of TMJ TJR on the masticatory muscles should be checked. | — |
Secondary
| Measure | Time frame |
|---|---|
| The study intends to decide on therapeutic measures for patients, treated as well as health policy decisions. | — |
Countries
Germany
Contacts
Public ContactSabine Linsen
Rheinische Friedrich-Wilhelms Universität Bonn,ZZMK-Zahnärztliche Prothetik
Outcome results
None listed