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Starting soon Not applicable

A Comparative Study of EMG Biofeedback and Pharmacotherapy for the Treatment of Masticatory Muscle Hyperactivity in Bruxism Patients

NCT06894472 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-03-26
Last updated
2025-03-25

Condition(s) studied

Bruxism

Investigational drug(s) / intervention(s)

Electromyography biofeedbackPharmacotherapy →

Electromyography biofeedback: Participants in the experimental group will receive surface electromyography (SEMG) feedback training, targeting the Masseter muscle, for 40 minutes per session according to the Evidence-Based practice since longer practice may become counterproductive due to fatigue and loss of focus. The frequency of the sessions will be 3 sessions/week for 4 weeks.

Pharmacotherapy: Pharmacotherapy will be received by all participants in the two groups in the form of multi relaxant (cyclobenzaprine) 10 MG twice daily for 4 weeks \& anti inflammatory (non steroidal anti-inflammatory drugs).

Study summary

This study examines the effect of electromyography biofeedback on masticatory muscles hyperactivity on patients with bruxism.

Eligibility

Sex
ALL
Min age
20 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Twenty adult subjects with definite mild to moderate bruxism examined by a dentist prior to the study. * Tenderness of masticatory muscles on palpation grade one and two according to the digital palpating scale * Mild to moderate myofascial pain around the temporomandibular joint causing discomfort in the morning. Exclusion Criteria: * Took any Botox or PRP injection treatment for this condition for the last six months * Had any advanced periodontal disease. * Any intraoral fixed splints. * Pregnancy. * Under psychiatric care. * Parkinson * Have any visual or auditory impairment. * Any cervical posture abnormalities.

Primary outcome measure(s)

  • Assessment of Masseter Hyperactivity — 4 weeks
    The assessment of Masseter muscle hyperactivity will be carried out by the digital palpating scale according to the following criteria: Grade Zero (0): when the muscle palpated and there is no pain or tenderness reported by the patient. Grade (1): Recorded if the patient response the palpation is uncomfortable (tenderness or soreness). Grade (2): is recorded if the patient experiences definite discomfort or pain. Grade (3): is recorded if the patient shows evasive action or eye tearing or verbalizes a desire not to have the area palpated again.

Trial sites (1)

FacilityCityRegionStatus
Misr University for Science and Technology Giza Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06894472 on ClinicalTrials.gov ↗ ← All trials in Egypt