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NCT06141863 Clinical Trial

Temporomandibular Dysfunction in Patients With Cervical Disc Herniation

Temporomandibular Joint Dysfunction Syndrome Clinical Trial

Official title:
Investigation of Temporomandibular Dysfunction in Patients With Cervical Disc Herniation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06141863
Other study ID # 6135131342/2022-28
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 1, 2022
Est. completion date December 30, 2022

Study information
Verified date November 2023
Source Karadeniz Technical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Cervical spine problems are associated with temporomandibular joint (TMJ) and related muscles.The aim of the present study was to investigate temporomandibular joint dysfunction (TMD) and pain in individuals with cervical disc herniation (CDH) according to the level of neck disability.

Description:

The study included diagnosed with cervical disc herniation. The participants were divided into two groups based on their The Neck Disability Index (NDI) score: Group 1 with no disability and mild disability and Group 2 with moderate and severe disability. Temporomandibular dysfunction and its severity, intensity of neck and temporomandibular joint pain was assessed.

Recruitment information / eligibility
Status Completed
Enrollment 60
Est. completion date December 30, 2022
Est. primary completion date November 30, 2022
Accepts healthy volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Diagnosed with cervical disc herniation aged between 18 and 65, - who could read and write in Turkish Exclusion Criteria: - Individuals with a history of head and neck surgery, fracture, physiotherapy or medical treatment cervical or temporomandibular joint treatment within the last six months, - presence of any inflammatory rheumatic diseases, such as ankylosing spondylitis and rheumatoid arthritis, facial paralysis, infection, advanced osteoporosis

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• questionnaire
Neck Disability Index, The Fonseca Anamnestic Index (FAI) and Visual Analogue Scale (VAS)

Locations
Country Name City State
Turkey Karadeniz Technical University Trabzon

Sponsors (1)
Lead Sponsor Collaborator
Karadeniz Technical University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Neck Disability Index Assessment of neck disability one day assessment
Primary Fonseca Anamnestic Index Assessment of temporomandibular dysfunction one day assessment
Secondary Visual Analogue Scale Assessment of temporomandibular joint pain and neck pain intensity one day assessment
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