RecruitingNot ApplicableNCT07576582

Peloid Therapy in Temporomandibular Joint Dysfunction

The Effect of Peloid Therapy on Pain and Functional Outcomes in Patients With Temporomandibular Joint Dysfunction


Sponsor

Uşak University

Enrollment

40 participants

Start Date

Apr 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This prospective, single-group clinical study will evaluate whether local peloid therapy improves pain and jaw function in adults with temporomandibular joint dysfunction. Participants will receive peloid therapy applied to the temporomandibular joint region and masticatory muscles for 20 minutes per session, 5 days per week, for 2 weeks. Pain and functional outcomes will be measured at baseline and at the end of treatment using validated clinical scales, including the Jaw Functional Limitation Scale-8, visual analog scale pain scores, Fonseca index, maximum mouth opening, and secondary otalgia assessment.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Inclusion Criteria1

  • Age between 18 and 65 years Diagnosis of temporomandibular joint dysfunction based on DC/TMD criteria Presence of TMJ-related pain for at least 4 weeks Baseline pain intensity ≥3 on a 0-10 visual analog scale Ability to provide written informed consent

Exclusion Criteria1

  • History of temporomandibular joint trauma, tumor, active infection, or acute inflammation Previous temporomandibular joint surgery Presence of systemic inflammatory rheumatologic disease Pregnancy Open wound, active dermatitis, or skin condition preventing peloid application at the treatment site Injection therapy (e.g., botulinum toxin) or regular physical therapy for TMJ within the past 3 months Any clinical or behavioral condition that may interfere with study compliance

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Interventions

OTHERLocal Peloid Therapy

Participants will receive local peloid therapy applied externally over the temporomandibular joint region and adjacent masticatory muscles. The treatment will be delivered as 10 sessions over 2 weeks, with 5 sessions per week. Each session will last 20 minutes. Peloid therapy will be administered by a trained investigator according to the study protocol.


Locations(1)

Uşak University Faculty of Medicine

Uşak, Merkez, Turkey (Türkiye)

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NCT07576582


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