the purpose of this study is to compare the effect of physical therapy (PT) program and oral
appliance on patients with temporomandibular disorder (TMD)-related myofascial pain (MFP).
Other: PT program
Device: oral appliance
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Full eligibility criteria for NCT01725867
Ages eligible for Study
20 Years to 65 Years
Genders eligible for Study
Accepts Healthy Volunteers
(1) 20-65 years old female, (2) diagnosed as MFP subtype of TMD according to Research Diagnostic Criteria for TMD (RDC/TMD), (3) pain duration over 3 month, (4) palpable taut band in masseter, (5) Asymmetrical pain intensity, (6) subsided symptoms of joint inflammation.
(1) traumatic TMD from external impact force, (2) history of traumatic cervical injury, (3) presence of systemic disease, (4) fibromyalgia, (5) co-interventions for cervical problems or TMD during study period, (6) signs of psychosomatic illness, (7) unwilling to be randomized, (8) unable to wear the splint or received intraoral myofascial release, (9)pregnancy.
All locations for NCT01725867
National Taiwan University Hospital
Taipei, Taiwan, 100
View full eligibility
Tris trial is registered with FDA with number: NCT01725867. The sponsor of the trial is National Taiwan University Hospital and it is looking for 49 volunteers for the current phase.
Official trial title: Comparing the Effect of Physical Therapy With Oral Appliance on Temporomandibular Disorder Related Myofascial Pain
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