DRKS00031209RecruitingUnknown
Clinical prospective study on the probation of additively manufactured bite splints in direct comparison to splints made of milled PMMA - Clinical probation of 3D printed bite splints
Johann Wolfgang Goethe-Universität Frankfurt am Main0 sites30 target enrollmentStarted: May 4, 2023Last updated:
Conditions
Trial Snapshot
- Phase
- Unknown
- Status
- Recruiting
- Enrollment
- 30
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized controlled study
- Masking
- Blinded (masking used)
Eligibility Criteria
- Ages
- 18 Years to Years (—)
- Sex
- All
Inclusion Criteria
- •Patients over 18 years of age, fully dentate or fixed prosthetic upper and lower jaw, indication for the preparation of a bite splint as a nightguard, presence of eccentric bruxism or other nocturnal parafunctions of the jaw with movement pattern - evidence by BruxCheck, no arthropathy of the temporomandibular joints requiring treatment, no planned need for dental treatment during the examination period - excluding teeth cleaning, signed consent and data protection declaration on a voluntary basis for participation in the study
Exclusion Criteria
- •Patients under 18 years of age, edentulous patients or patients treated with removable dentures, no presence of bruxism or other nocturnal parafunctions of the jaw, arthropathy of the temporomandibular joints requiring treatment, dental treatment required during the study period - with the exception of tooth cleaning, lack of consent and data protection declaration, participation in the planning and implementation of the study, Presence of alcohol or drug abuse, Uncontrolled pathological processes in the oral cavity, Mental or psychosomatic illness that would affect participation in the study and compliance with the study protocol.
Investigators
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