Temporomandibular Joint Disorders Clinical Trial
Official title:
Comparing the Effect of Typical Electrical Stimulation Therapy With Nocipoint Stimulation Therapy on TMD-Related Myofascial Pain
The purpose of this study is to measure the effect of nocipoint therapy on patients with temporomandibular joint disorders (TMD) and compare it with the effect of standard electrical stimulation therapy.
The prevalence of temporomandibular disorders (TMD) is about 20% to 60% of dental patients.
Most patients suffer from myofascial pain (MFP) subtype of TMD. Analgesics, local muscle
injection or oral appliance are often used to treat TMD-related MFP. Patients are also
referred to physical therapists frequently. Many physical therapy (PT) modalities and
techniques are applied to these patients, including non-invasive transcutaneous electrical
nerve stimulation (TENS) using TENS devices. However, the exact application of TENS devices,
including the location of the stimulation, duration and intensity of stimulation, is largely
decided by physical therapists. Nocipoint Therapy, a unique combination of precise location,
duration and intensity of TENS has been found to substantially relieve general myofascial
pain and recover the muscle function with lasting effect.
In preliminary observations of clinical applications, Nocipoint Therapy has been found to
rapidly and substantially relieve TMD-related MFP within 2-3 sessions of the treatment.
This clinical study compares the effect of Nocipoint Therapy on TMD with that of standard
Physical therapy (PT). TENS will be used in the control group both as a part of the standard
of care (i.e., PT) and as placebo.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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