RecruitingNot ApplicableNCT07321483

Reflex Therapy of Temporomandibular Dysfunctions

Evaluation of the Therapeutic Efficacy of Reflex Therapy Using Dry Needling in Patients With Functional Temporomandibular Pain Syndrome: A Prospective, Randomized, Controlled Pilot Study.

Sponsor

Palacky University

Enrollment

100 participants

Start Date

Sep 20, 2025

Study Type

INTERVENTIONAL

Conditions

Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders

Summary

This study aims to evaluate the effectiveness of dry needling in patients with functional temporomandibular pain syndrome by comparing standard rehabilitation therapy alone with therapy combined with dry needling to reduce pain, improve jaw function and enhance quality of life.

Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a procedure called Dry needling and a procedure called Standard rehabilitation for people with temporomandibular joint dysfunction; myofascial pain syndrome; orofacial pain; musculoskeletal disorders. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREDry needling

One dry needling intervention targeting trigger points in the masseter and temporalis muscles during the first treatment session

PROCEDUREStandard rehabilitation

The therapy will include mobilization, soft tissue relaxation techniques, and specific exercises focused on improving temporomandibular joint mobility and reducing muscle tension.

Locations(1)

Faculty of Health Sciences, Palacký University Olomouc, Czech Republic

Olomouc, Czechia

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NCT07321483