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NCT07321483

Reflex Therapy of Temporomandibular Dysfunctions

Recruiting now NA Last updated 7 January 2026
What this trial tests

NA trial testing Dry needling in Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders in 100 participants. Currently enrolling.

Timeline
20 September 2025
Primary endpoint
1 July 2026
2 August 2026

Quick facts

Lead sponsorPalacky University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment100
Start date20 September 2025
Primary completion1 July 2026
Estimated completion2 August 2026
Sites1 location across Czechia

Drugs / interventions tested

Conditions studied

Sponsor

Palacky University

Who can join

18 and older, any sex, with Temporomandibular Joint Dysfunction; Myofascial Pain Syndrome; Orofacial Pain; Musculoskeletal Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Dry needling

Trials testing the same drug.

Other Palacky University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07321483.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing