Diagnostic and Prognostic Salivary Biomarkers in Chronic Muscle Pain
1 other identifier
observational
160
1 country
1
Brief Summary
A large proportion of the adult population worldwide currently lives with chronic muscle pain, with more than half of those affected experiencing pain localized to the face and jaw. This means that approximately 10-15% of the adult population is affected. Living with chronic muscle pain impacts many aspects of life, significantly affecting both the individual's quality of life and well-being as well as that of their close relations. As with other chronic pain conditions, researchers agree that multiple factors contribute to the development and aggravation of the condition. The aim of this project is to identify proteins in saliva that are involved in the disease process of chronic muscle pain, in order to better understand the underlying mechanisms, improve prognosis assessment, and ultimately develop more effective treatments. The project includes patients with localized chronic jaw muscle pain, those with generalized chronic pain (fibromyalgia), and pain-free individuals in a matched control group. Validated questionnaires are used to assess pain, including measures of physical and emotional function, followed by a clinical examination. Chewing-stimulated saliva is selected for sampling based on previous studies from the research group, and blood samples are collected from all participants. Proteins involved in metabolism, stress, and immunity will be analyzed, building on prior research conducted by the group. Patients will undergo conventional orofacial pain treatment and will later be followed up with new samples to study changes in protein expression following successful treatment. Chronic muscle pain is one of the leading causes of work incapacity and long-term sick leave. This project combines clinical examinations with advanced biomedical analysis methods to investigate the role of specific proteins in disease development. The goal is to identify proteins involved in pain mechanisms to improve diagnostics and enable personalized treatments. In the short term, this could lead to faster and more accurate diagnoses and the development of new treatment strategies, which would reduce pain intensity and work incapacity, ultimately benefiting both individuals and society.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2023
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
September 1, 2023
CompletedFirst Submitted
Initial submission to the registry
May 20, 2025
CompletedFirst Posted
Study publicly available on registry
May 29, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2029
June 4, 2025
May 1, 2025
3.6 years
May 20, 2025
May 30, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Change in salivary protein expression levels
Change in salivary protein expression levels (e.g., inflammation-, stress-, or metabolism-related biomarkers) before and after conventional orofacial pain treatment,
7 months
Study Arms (2)
Muscle pain
Patients diagnosed with myogenious TMD and patients diagnosed with Fibromyalgia according to ACR 1990/2016
Control
Matched healthy controls
Eligibility Criteria
Participants will be recruited through advertisement and from patients referred to the specialist clinic for orofacial pain and jaw function at the University Dental Clinic at Karolinska Institute (Huddinge, Sweden) and at Eastman Institutet, Folktandvården Stockholm.
You may qualify if:
- Diagnosis of myalgia or myofascial pain with referral according to the DC/TMD Axis I
- Diagnosis of fibromyalgia according to ACR 1990 or ACR 2016 criteria
- Minimum pain intensity of 30 on a 100 mm visual analogue scale (VAS)
You may not qualify if:
- Diagnosed systemic muscular or joint diseases (except for fibromyalgia)
- Whiplash-associated disorder
- Migraine
- Neurological disorders
- Neuropsychiatric disorders
- Diseases of the salivary glands (e.g., sialadenitis, salivary gland tumours)
- Pregnancy and lactation
- Obesity
- Use of analgesics within the last 24 hours
- Oral complaints such as oral dryness
- Mucosal lesions in the oral cavity
- Fewer than 22 natural teeth
- Extensive prosthodontic rehabilitations
- Poor oral hygiene
- Hyposalivation
- +2 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Karolinska Institutetlead
- Eastmaninstitutetcollaborator
Study Sites (1)
Karolinska Institutet, Department of Dental Medicine
Stockholm, Huddinge, 14152, Sweden
Biospecimen
Saliva, blood
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
May 20, 2025
First Posted
May 29, 2025
Study Start
September 1, 2023
Primary Completion (Estimated)
April 1, 2027
Study Completion (Estimated)
January 1, 2029
Last Updated
June 4, 2025
Record last verified: 2025-05