跳至主要内容
临床试验/DRKS00018092
DRKS00018092已完成未知

Comparison of treatment outcome with a full-occlusion biofeedback splint on sleep bruxism and TMD pain compared to treatment with an adjusted occlusal splint - biofeedback study bruxism

Poliklinik für Zahnärztliche Prothetik LM0 个研究点目标入组 41 人开始时间: 2020年5月6日最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
41

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
Open (masking not used)

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • (1) physical signs of bruxism visible on the dentition (grinding facets, abnormal tooth wear and/or wedge-shaped lesions)
  • (2) self-reported pain in the masticatory muscles and/or the temporomandibular joint (TMJ”)
  • (3) willingness of the patient to participate in the study and a commitment to adhere to the pre-set timetable.

排除标准

  • (1) acute pain caused by other components of the masticatory system (e.g. caries, root inflammation)
  • (2) prior or planned TMJ or dysgnathia surgery
  • (3) jaw fractures, (4) otorhinolaryngologic diseases (except tinnitus), (5) systemic basic illness with rheumatic origin e.g. arthritis, arthrosis, gout and psoriasis, (6) psychosomatic or psychiatric diseases, (7) implanted electronic devices, (8) arrhythmia and other (prior or present) cardiac problems, (9) epilepsy, (10) cerebrovascular and brain diseases, (11) pregnancy including breastfeeding period, (12) drug or alcohol abuse, analgesic or sedative therapy, use of medication affecting the central nervous system (e.g. antidepressants, anxiolytics and anticonvulsants), (13) physical or mental disability, (14) maxillary hyperesthesia and/or allergy to materials used, (15) missing support zones in the posterior region or anatomical topography which made a full-coverage maxillary splint impossible to use, (16) a past history of received biofeedback therapy and (17) insufficient recorded bruxing activity in the baseline phase

研究者

发起方
Poliklinik für Zahnärztliche Prothetik LM

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