NCT07321483 Reflex Therapy of Temporomandibular Dysfunctions
| NCT ID | NCT07321483 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Palacky University |
| Condition | Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders |
| Study Type | INTERVENTIONAL |
| Enrollment | 100 participants |
| Start Date | 2025-09-20 |
| Primary Completion | 2026-07-01 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 100 participants in total. It began in 2025-09-20 with a primary completion date of 2026-07-01.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief 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 Criteria
Inclusion Criteria: * Diagnosed with functional temporomandibular pain syndrome without structural temporomandibular joint damage. * Aged ≥18 years. * Stable health condition suitable for outpatient rehabilitation. * Willingness to participate and ability to follow the therapeutic protocol. Exclusion Criteria: * Presence of degenerative, post-traumatic, or inflammatory changes in the temporomandibular joint. * Cognitive or psychiatric disorders limiting cooperation. * Lack of informed consent or non-compliance during treatment
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07321483 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07321483 currently recruiting?
Yes, NCT07321483 is actively recruiting participants. Contact the research team at petr.konecny@upol.cz for enrollment information.
Where is the NCT07321483 trial being conducted?
This trial is being conducted at Olomouc, Czechia.
Who is sponsoring the NCT07321483 clinical trial?
NCT07321483 is sponsored by Palacky University. The trial plans to enroll 100 participants.