Actively Recruiting
Reflex Therapy of Temporomandibular Dysfunctions
Led by Palacky University · Updated on 2026-01-07
100
Participants Needed
1
Research Sites
45 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Reflex Therapy of Temporomandibular Dysfunctions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with functional temporomandibular pain syndrome without structural temporomandibular joint damage.
- Aged 18 years or older.
- Stable health condition suitable for outpatient rehabilitation.
- Willingness to participate and ability to follow the therapeutic protocol.
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Faculty of Health Sciences, Palacký University Olomouc, Czech Republic
Olomouc, Czechia, 77900
Actively Recruiting
Research Team
P
Petr Konečný, Ph.D, M.D., assoc.prof.
CONTACT
D
Dana Dvořáková, MSc.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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