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临床试验/CTRI/2026/02/104397
CTRI/2026/02/104397尚未招募不适用

Comparison of the efficacy of a muscle relaxant-Tizanidine with Low level laser therapy in treatment of Myofascial and TMJ pain dysfunction syndrome

Rupak Biswas1 个研究点 分布在 1 个国家目标入组 48 人开始时间: 2026年3月2日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
48
试验地点
1

研究概览

简要总结

This study will include patients attending the outpatient department of Oral and Maxillofacial Surgery with symptoms of myofascial pain dysfunction syndrome and temporomandibular joint disorders such as pre auricular pain reduced mouth opening muscle tenderness and TMJ sounds. All eligible patients will be enrolled after thorough history taking with special attention to any past allergic reactions to muscle relaxants or analgesics.

After obtaining informed consent patients will be randomly divided into two groups. Group A will receive red light therapy using a low level laser of 660 nm wavelength for three minutes per session three times per week for two weeks along with diclofenac as rescue medication. Group B will receive tizanidine four milligrams once daily for two weeks along with diclofenac as rescue medication. All medications will be provided free of cost.

Baseline assessment will include pain evaluation using visual analog scale measurement of mouth opening and assessment of TMJ sounds. Patients will be followed up on day seven day fourteen and up to one month after treatment to evaluate pain reduction improvement in jaw mobility muscle relaxation and TMJ sounds. Patients will also report the number of diclofenac tablets consumed which will be recorded for analysis.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Outcome Assessor Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • 1.Individuals diagnosed with TMJD and MPDS.
  • 2.Age between 18 to 60 years.
  • 3.Individuals willing to participate in the study.

排除标准

  • 1.Pregnant or breastfeeding women.
  • 2.Individuals with any neurological disorders.
  • 3.Those Individuals who are undergoing concurrent TMJ surgeries or interventions.
  • 4.Individuals with history of trauma in TMJ region.
  • 5.Individuals allergic to medications proposed to be used in the study sensitive to red light.

研究者

发起方
Rupak Biswas
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Rupak Biswas

NAIR HOSPITAL DENTAL COLLEGE

研究点 (1)

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