跳至主要内容
临床试验/NCT01005511
NCT01005511终止不适用

A Single Centre, Randomised, Clinical Placebo Controlled Study of the Optimal Treatment and Long-term Effect of FES on Sleep Bruxism

Medotech A/S2 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2009年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
48
试验地点
2
主要终点
Reduction in the electromyography (EMG) activity per hour per night

研究概览

简要总结

To investigate the effect of the treatment with Grindcare® on the muscles- and jaw symptoms and at the jaw muscle activity during sleep.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signed and dated ICF
  • 18 years or older
  • Fulfill the RDC-criteria for myofascial TMD diagnose (group 1a or 1b)

排除标准

  • Contraindication of concommitant diseases for the study judged by investigator
  • Patients who are using occlusal splints in the treatment period.

结局指标

主要结局

Reduction in the electromyography (EMG) activity per hour per night

时间窗: 10 weeks after start of treatment

次要结局

  • Evaluation of long-term effect of FES on the EMG activity(a 4 weeks period after end og treatment with FES)

研究者

发起方
Medotech A/S
申办方类型
Industry

研究点 (2)

Loading locations...

相似试验