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Clinical Trial Summary

Evaluating myofascial pain dysfunction symptoms using acupuncture, dry needle and Botox injection using electromyography and visual Analogue Scale on two time intervals at 2 and 6 months after the intervention


Clinical Trial Description

All the patients will be selected and examine from the outpatient clinic of Oral and Maxillofacial surgery department. Faculty of Dentistry, Cairo University, Egypt. Electromyography examination will be conducted in the department of neurophysiology department. faculty of Medicine, Cairo University, Egypt. Adult patients of both sexes, aged from 15 to 60 years with myofascial pain dysfunction syndrome complaining from sign and symptoms of pain or muscles spams and examination shows trigger points in masticatory muscles. selected patients must have not received any other form of surgical treatment related to TMJ disorders All patients involved in this study will be divided into three groups, each group will receive a technique for one side of MPDS, involving acupuncture, dry needle, and Botox injection. for both, acupuncture group and dry needling group, patients should receive a session/week for 4-6 weeks ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06013644
Study type Interventional
Source Cairo University
Contact
Status Recruiting
Phase Early Phase 1
Start date June 3, 2023
Completion date February 1, 2024

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