Acupuncture, Dry Needle and Botox Injection in Management of Patient With Myofascial Pain Dysfunction Syndrome

Early Phase 1UnknownNCT06013644

Cairo University39 enrolled

Overview

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

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 Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Myofascial Trigger Point Pain Myofascial Pain Syndrome

Interventions

Acupuncture needleDEVICE

a weekly session for 4-6 weeks on needle for each acupoint for at least 20 minutes the included acupoints are ST6, ST7, SI 18, ST 19, GB 2

Dry needleDEVICE

a weekly session for 4-6 weeks the trigger point is held by thumb and index fingers and the needle approaches the point perpendicular to the skin and rotated clockwise for 2-3 minutes

Botox Injectable ProductDRUG

each patient will receive a one time treatment of a suitable dose (estimated by the research team) according to the severity of the symptoms

Eligibility

Sex: ALLMin age: 15 YearsMax age: 60 YearsHealthy volunteers:

Medical Language ↔ Plain English

Accepts Healthy Volunteers Inclusion Criteria: * Healthy Volunteers * MPDS patient * Adult patients of both sexes, aged from 15 to 60 years * signs and symptoms of pain or muscles spams * Trigger points in masticatory muscles * Patients had not received any other form of surgical treatment related to TMJ disorders * Cooperative patient Exclusion Criteria: * Severe bleeding tendency, e.g. anticoagulant therapy, thrombocytopenia * Edentulous patients, and total dental prosthesis. * Psychologically disturbed and mental disturbance patients * major systemic disorders (- Valvular heart disease: avoid indwelling needles) * seizure patients * A confirmed or suspected diagnosis of an inflammatory disorder and autoimmune. * Patient on Medication (insulin- corticosteroids, nonsteroidal anti-inflammatory therapy or narcotics, muscle relaxants, herbal medicines.) * Analgesic or anti-depressants over the last 2 weeks. * Any anatomical abnormality in TMJ. * Pregnant women. * Allergies to metals.

Locations (1)

Wajma Sayed Karim Al Sayed

Cairo, Egypt

RECRUITING

Outcomes

Primary Outcomes

change of electrical activity of mastication muscles from the baseline measurement

change of electrical activity of mastication muscles from the baseline measurement through assessment of muscle tone using electromyography (EMG) in microvolts and refer to the behavior of muscles: at (rest /open, chewing, clenching)

Time frame: 2 months after treatment

change of electrical activity of mastication muscles from the baseline measurement

Time frame: 6 months after treatment

Secondary Outcomes

change of Pain perception from baseline measurement during maximum mouth opening in millimetres and rest by a Visual Analog Score (where Zero means no pain and 10 means the worst pain possible)

change of Pain perception from the baseline measurement during maximum mouth opening in millimetres and rest by a Visual Analog Score (where Zero means no pain and 10 means the worst pain possible)

Time frame: 2 months after treatment

change of Pain perception from baseline measurement during maximum mouth opening in millimetres and rest by a Visual Analog Score (where Zero means no pain and 10 means the worst pain possible)

change of Pain perception from the baseline measurement during maximum mouth opening in millimetres and rest by a Visual Analog Score (where Zero means no pain and 10 means the worst pain possible)

Time frame: 6 months after treatment

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.