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Clinical Trials/NCT06488937
NCT06488937
Active, not recruiting
Not Applicable

Determinants of Orofacial Pain and Temporomandibular Disorders in People With Rheumatoid Arthritis

Josip Juraj Strossmayer University of Osijek1 site in 1 country92 target enrollmentNovember 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Temporomandibular Disorders
Sponsor
Josip Juraj Strossmayer University of Osijek
Enrollment
92
Locations
1
Primary Endpoint
levels of calcium (Ca), magnesium (Mg), phosphate (P), uric acid, alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) and gamma- glutamyltransferase (GGT) in serum
Status
Active, not recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this observational study is to determinate temeporomandibular disorders (TMDs) and levels of biomarkers in 30 rheumatoid arthritis patients and 30 healthy controls.

Aims are:

  • to determine TMDs symptoms in both groups using a validated Reasearch Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) protocol
  • to determine levels of interleukin-4 (IL-4), interleukin-18 (IL-18) and interferon-gamma (IFN-γ) in saliva and serum in RA patients and control group
  • to determine levels of biomarkers (Ca, Mg, P, AST,ALT,ALP,GGT,urate) in serum of RA patients and control group
  • investigate the correlation between cytokines level in saliva and serum
  • to determine the effect of TMDs on cytokine and biomarker levels Participants will be clinicaly examined by DMD in accordance with the RDC/TMD guidelines to receive both Axis I and Axis II diagnoses. After examination participants would be asked for saliva and blood sample.

Detailed Description

Rheumatoid arthritis (RA) is chronic inflammatory autoimmune disease characterized by symmetrical peripheral polyarthritis with consequent joint destruction. Predominantly affecting wrist and foot joints, RA can also affect temporomandibular joint (TMJ) causing temporomandibular disorders (TMDs). 4-80% of RA patients suffer from TMDs. It remains unclear why some RA patients do not have TMDs and don't suffer from orofacial pain, depression and somatization. The present study was therefore designed to explore the level of cytokines and biochemical parameters from saliva and serum in RA patients and control participants to examine their correlation with TMDs. Study results could provide valuable insights for the understanding of the orofacial pain and depression onset in RA patients Participants would be examined by a non-blinded examiner with knowledge to which group the patient was in. After intraoral examination Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) will be used as an international diagnostic protocol for TMDs. Assessment included clinical examination of TMJs and masticatory muscles with measurement of mandibular dynamics. The participants will be requested to spit 2 mL of unstimulated saliva into a sterile tube with their head slightly bended forward. Saliva samples were stored at -20℃ until analysis. Blood samples will be collected in Vacutaners. Serum calcium (Ca), magnesium (Mg), phosphate (P), uric acid, alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) and gamma-glutamyltransferase (GGT) were measured up to 6 hours after collection. Serum aliquots were stored at -20℃ until cytokine analysis. An Invitrogen assays were used to analyze salivary and serum concentration of IL-4,IL-18 and IFN-γ.

Registry
clinicaltrials.gov
Start Date
November 1, 2019
End Date
February 2025
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matea Dozet

DMD

Josip Juraj Strossmayer University of Osijek

Eligibility Criteria

Inclusion Criteria

  • Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study
  • Patients diagnosed with RA according to 2010 ACR-EULAR RA criteria.

Exclusion Criteria

  • Refusal to sign informed consent form
  • Diagnosed chronic systemic disease
  • Any infection including TB, HIV, Hepatitis B or C
  • Malignancy
  • Pregnancy

Outcomes

Primary Outcomes

levels of calcium (Ca), magnesium (Mg), phosphate (P), uric acid, alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP) and gamma- glutamyltransferase (GGT) in serum

Time Frame: baseline

measured up to 6 hours after collection on Roche Cobas c501 biochemistry analyzer

levels of cytokines IL-4, IL-18, IFN-γ in serum

Time Frame: baseline

Invitrogen assays will be used for multicomplex quantitative analysis of inflammatory mediators. The entire protocol will be carried out according to the instructions of the manufacturer of Thermofischer Scientific

levels of cytokines IL-4, IL-18, IFN-γ in saliva

Time Frame: baseline

Invitrogen assays will be used for multicomplex quantitative analysis of inflammatory mediators. The entire protocol will be carried out according to the instructions of the manufacturer of Thermofischer Scientific

Study Sites (1)

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