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临床试验/NCT00936338
NCT00936338已完成不适用

Randomized Clinical Trial of Treatment for Temporomandibular Joint (TMJ) Disc Displacement

Tokyo Medical and Dental University1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2006年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
44
试验地点
1
主要终点
(i) maximum mouth opening range without and (ii) with pain, (iii) present pain intensity, and (iv) limitation of daily activities

研究概览

简要总结

The effectiveness of physical therapy for treatment of anterior disc displacement without reduction of temporomandibular disorders has not been well defined. This study compared the treatment method with conservative splint therapy. Fifty two subjects were assigned at random to either of two treatment groups: one is a splint treatment group, and the other is a joint mobilization self exercise group. Each treatment was evaluated using four outcome variables: (i) maximum mouth opening range without and (ii) with pain, (iii) present pain intensity, and (iv) limitation of daily activities. All outcome variables were significantly improved after eight-week of treatment in the exercise group. Meanwhile, the splint treatment improved three variables, other than "mouth opening with pain"; however, the degree of improvement was less than that seen in the exercise group. This result demonstrates that the joint mobilization self exercise improves jaw function and relieves pain as compared to the splint treatment.

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

  • (1) male or female over 18 years old;
  • (2) with mouth opening pain on the TMJ affected side;
  • (3) over two weeks after the onset of ADDwoR;
  • (4) with maximum mouth opening of less than 40 mm; and
  • (5) MRI-confirmed ADDwoR. The

排除标准

  • (1) unwilling or unable to receive splint and/or exercise therapy;
  • (2) with systemic bone or joint disease,
  • (3) regular medication such as analgesics, anti-anxiety drugs, antidepressants and psychotropics; and
  • (4) missing teeth and/or a removable denture but having a fixed partial denture restoration over one year.

结局指标

主要结局

(i) maximum mouth opening range without and (ii) with pain, (iii) present pain intensity, and (iv) limitation of daily activities

时间窗: 0, 4 and 8 week

次要结局

未报告次要终点

研究者

申办方类型
Other

研究点 (1)

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