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临床试验/NCT06675149
NCT06675149已完成不适用

Effect of Diacutaneus Fibrolysis on Tempromandibular Joint Pain and Trismus Post Oral and Maxillofacial Surgery

Cairo University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年8月20日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
1
主要终点
temporomandibular joint pain

研究概览

简要总结

This study is carried out on sixty patients who will have tempromandibular pain and trismuspostOral and Maxillofacial Surgeryand their ages will be ranged from 18 to 40 years.

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
None

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Ages of patients will be ranged from 18 to 40 years.
  • •All patients will have Oral and Maxillofacial Surgery.
  • •All patients will be referred by a surgeon before starting the study procedure.
  • •All participants will have pain and trismus in the jaw,
  • •The participants will be also cleared for periodontal issues.
  • •All patients will enter the study having their informed consent

排除标准

  • •Patients with associated vascular injuries requiring arterial repair.
  • •Patient with systemic diseases such as arthritis; pain attributable to confirmed migraine, head, or neck pain condition
  • •Patient with acute infection or other significant disease of the teeth, ears, eyes, nose, or throat
  • •Patient with present neurologic or cognitive deficit.
  • •Patients with history of previously failed surgeries.

研究组 & 干预措施

Group B

Experimental

This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .

干预措施: Diacutaneus fibrolysis (Device)

Group B

Experimental

This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .

干预措施: Transcutaneous electrical nerve stimulation (Device)

Group B

Experimental

This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .

干预措施: Massage (Procedure)

Group A

Placebo Comparator

This group will includes 30 patients who will receive 4 weeks (3times/week) post-surgical traditional physiotherapy (TENS , massage , range of motion exercise ) .

干预措施: Transcutaneous electrical nerve stimulation (Device)

Group A

Placebo Comparator

This group will includes 30 patients who will receive 4 weeks (3times/week) post-surgical traditional physiotherapy (TENS , massage , range of motion exercise ) .

干预措施: Massage (Procedure)

结局指标

主要结局

temporomandibular joint pain

时间窗: pre intervention and re assessed after 1 month

pain is assessed Pressure pain threshold(PPT) will be obtained with the aid of an algometer by applying pressure to the masseter and to the anterior, middle, and posterior temporalis, increasing pressure until the patient will feel that the pressure will become unpleasant or "painful .

Trismus

时间窗: pre intervention and re assessed after 1 month

Trismus is assessed by caliper

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Aliaa Elsayed Ali

Demonstrator

Cairo University

研究点 (1)

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