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临床试验/DRKS00008848
DRKS00008848招募中2 期

Study to compare the effects between the RelaxBogen and its Myo fascial approach with the occlusial splint in TMD and Bruxism therapie - RB2

Zahnarztpraxis0 个研究点目标入组 34 人开始时间: 2016年9月16日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
34

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • 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

排除标准

  • 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.

研究者

发起方
Zahnarztpraxis

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