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The study will determinate influence of four selected physiotherapeutic procedures on the pain intensity and the range of mandibular mobility in patients with myofascial disorders in the SS.
Full description
The study group will consist of 100 women (GI) aged 20 to 45 who report pain and increased facial muscle tension in masseter muscles.
The diagnosis will be made according to RDC/TMD (Research Diagnostic Criteria for Temporomandibular Disorders), which will determine the occurrence of painful myofascial disorders. Patients will undergo both external and intraoral dental examinations to exclude odontogenic and articular causes of pain. Patients will then be palpated for the masseter muscles and both: the range of mandibular abduction (linear measurement in mm) and the level of pain intensity (VAS scale).
The control group (GII) will consist of 100 women between 20 and 45 years of age with no signs of masticatory disorders or orofacial pain during a physical examination and with no such reference in their medical records.
In order to obtain a homogenic study group the following inclusion criteria will be applied:
Exclusion criteria:
Patients with a stomatognathic system disorder will be randomized into four therapeutic subgroups, 26 patients each, who will receive a physiotherapy treatment of the masseter muscles for a period of 10 days (excluding Saturdays and Sundays). The duration of a single therapy session will be 12 minutes per patient in each of the subgroups.
The division of the study group into subgroups is as follows:
Immediately after the therapy, the patients' pain level will be assessed via VAS scale. After the last day of physiotherapy, a linear measurement of mandibular abduction will be performed.
Enrollment
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Inclusion criteria
I. Myofacial pain of less than 12 months in duration that is evoked by an active motion of the mandible or by palpation.
II. Diagnosis according to RDC / TMD (Research Diagnostic Criteria for Temporomandibular Disorders), which showed painful myofascial disorders III. A feeling of an increased muscle tension IV. Presence of all occlusal contact zones V. Female sex
Exclusion criteria
I. Past or present, neurological disease, neuromuscular disease or a severe systemic disease.
II. Temporomandibular joint pathology based on X-ray imaging or stomatological examination.
III. Orthodontic or prosthetic treatment IV. Contraindication to physiotherapeutic treatment
Primary purpose
Allocation
Interventional model
Masking
100 participants in 4 patient groups
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Central trial contact
Magdalena Gębska, PhD
Data sourced from clinicaltrials.gov
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