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NCT05740826 Clinical Trial

Correlation Between Cervical Spine Muscle Disorders and the Occurrence of Symptoms of Temporomandibular Joint Dysfunction

Temporomandibular Joint Disorders Clinical Trial

Official title:
Correlation Between Cervical Spine Muscle Disorders and the Occurrence of Symptoms of Temporomandibular Joint Dysfunction

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05740826
Other study ID # 676/22
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 8, 2022
Est. completion date December 30, 2022

Study information
Verified date February 2023
Source Poznan University of Medical Sciences
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study evaluated the correlation between the occurrence of disorders of selected muscles of the cervical spine and the occurrence of symptoms of TMJ dysfunction

Description:

The examination includes personal questionnaire, physical examination and an algometer measurement on the upper fibers of the trapezius, levator scapula, sternocleidomastoid and rectus capitis posterior major to define pressure sensitivity of neck muscles and define is there a correlation between the occurrence of disorders of selected muscles of the cervical spine and the occurrence of symptoms of TMJ dysfunction.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date December 30, 2022
Est. primary completion date December 30, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 19 Years to 25 Years
Eligibility Inclusion Criteria: - age 19-25 years - relatively good health - consent to participate in the research experiment Exclusion Criteria: - people with skin problems in the head and neck area that that made the examination impossible - previous head and neck surgeries and traffic injuries - coagulation disorders or taking medications that reduce blood coagulability - venous thrombosis in the neck area - sensory disorders - dislocation of the jaw in the past - taking painkillers 12 hours before starting the study - being under orthodontic or physiotherapeutic treatment focused on TMJ dysfunctions

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Algometer
The algometer head was applied to the trigger point of selected muscles at an angle of 90° and, increasing the pressure at a speed of about 100g/s, three measurements were made. Each measurement stoped at the first sensation of pain

Locations
Country Name City State
Poland Clinic for Rehabilitation Poznan Wielkopolskie

Sponsors (1)
Lead Sponsor Collaborator
Poznan University of Medical Sciences

Country where clinical trial is conducted

Poland, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pressure sensitivity Algometer measurements on the upper fibers of the trapezius, levator scapula, sternocleidomastoid and rectus capitis posterior major for each participant duration of test is about 30-40 minutes
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