Wear behavior of 3D printed and milled occlusal splints: A Randomized Pilot Study (CAMOS study).
Phase 3
Recruiting
- Conditions
- BruxismMyofascial pain of masticatory musclesTemporomandibular joint pain
- Registration Number
- DRKS00030792
- Lead Sponsor
- niversitätsklinikum Heidelberg, Abteilung für Zahnärztliche Prothetik
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Ability of the patient to give informed consent
Presence of the subject's informed consent.
Presence of TMD diagnosed according to the DC/TMD and, if applicable, confirmed by MRI findings, for which therapy using an occlusal splint is indicated. Alternatively: Presence of probable bruxism.
Exclusion Criteria
-therapy by means of an occlusal splint was not tolerated in the past.
- Patients who will not be able to attend the study appointments in time
- Denture wearers or partially edentulous patients with loss of support zones
- Pronounced bite position anomalies, which require a splint thickness of more than five mm
or require splint therapy in the mandible
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wear of occlusal splints after three months
- Secondary Outcome Measures
Name Time Method Technical complications