DRKS00008848RecruitingPhase 2
Study to compare the effects between the RelaxBogen and its Myo fascial approach with the occlusial splint in TMD and Bruxism therapie - RB2
Zahnarztpraxis0 sites34 target enrollmentStarted: September 16, 2016Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 2
- Status
- Recruiting
- Sponsor
- Enrollment
- 34
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 one (—)
- Sex
- All
Inclusion Criteria
- •N=34 with bruxism and TMD symptomes measured with a Bruxchecker Film and a TMD investigation by the dentist and with scientific questionaire.
- •Each patient needs to have, scince minimum of 3 months, an occlusal splint. An other selection criteria is, that the reason for the TMD and Bruxism is restricted to jaw, neck and shoulder pain.
- •The patients needs to be full aged and need to have no pschological disease.
- •People which suffue from an alcohol- oder drug disease are eccluded too
Exclusion Criteria
- •Exclusion criteria are:
- •The patient is underaged or not able to give one's consent. Used a RelaxBogen before. Is depressive, a drug abuser or takes medicine that could introduce Bruxism. A trauma in the head area or the cervical spine. Planned dental restoration during the period of the study. The main pain perception analysed in the SLNR-questionaire is not located in the area of the head, shoulders or the neck.
Investigators
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