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Based on surface electromyography to evaluate the clinical efficacy of extracorporeal shock wave therapy for temporomandibular joint disorder

Based on surface electromyography to evaluate the clinical efficacy of extracorporeal shock wave therapy for temporomandibular joint disorder - Observation of the clinical efficacy of shock wave therapy for temporomandibular joint disorder

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400090663
Enrollment
Unknown
Registered
2024-10-11
Start date
2024-10-12
Completion date
Unknown
Last updated
2024-10-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temporomandibular joint disorder

Interventions

control group:Conventional rehabilitation treatment, including ultrashort wave therapy, low-frequency pulse electrical therapy and manual therapy, is administered 6 times a week for a total of 3 weeks
Low-frequency shock wave group :On the basis of conventional rehabilitation treatment, low-frequency shock wave therapy is given. The shock wave parameters are: the frequency is 8 - 10 Hz, the treatm
High-frequency shock wave group:On the basis of conventional rehabilitation treatment, high-frequency shock wave therapy is administered. The shock wave parameters are: the frequency is 8 - 10 Hz, the

Sponsors

The First Department of Rehabilitation Medicine, the Second Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Ages ranging from 16 to 55 years old, meeting the DC/TMD Axis I diagnostic criteria released by the International Association for Dental Research in 2014; (2) Meeting the type I painful diseases in the DC/TMD Axis I diagnostic criteria, including: muscle pain (localized myalgia, myofascial pain, referred myofascial pain), arthralgia; as well as clinical manifestations such as abnormal mandibular movement, temporomandibular joint noises, etc.; (3) No space-occupying lesions were found in the temporomandibular joint imaging examination; (4) The patient has no severe malocclusion, good periodontal tissue, relatively complete dentition, and no bad prosthesis; (5) Has not received any treatment for TMD in the past 3 months; (6) Signed the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Abnormal temporomandibular joint activity or pain caused by tumors, systemic infections, or specific infections of the temporomandibular joint; (2) Rheumatoid temporomandibular arthritis; (3) Joint disorders that occur after traumatic arthritis or surgical operations; (4) Joint disorders that occur after tooth extraction or dental orthodontics; (5) Patients do not cooperate with treatment or have cognitive dysfunction and are unable to complete the questionnaire survey; (6) Neuromuscular system diseases.

Design outcomes

Primary

MeasureTime frame
Maximum Mouth Opening;Craniiomandibular Index;surface electromyography;—

Countries

China

Contacts

Public ContactNi Guangxiao

The Second Hospital of Hebei Medical University

ngx7912156@163.com+86 136 3321 0055

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026