NCT06994156

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P50-P75 for all trials

Timeline
32mo left

Started Sep 2023

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

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 Progress50%
Sep 2023Jan 2029

Study Start

First participant enrolled

September 1, 2023

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

May 20, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

May 29, 2025

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2027

Expected
1.8 years until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2029

Last Updated

June 4, 2025

Status Verified

May 1, 2025

Enrollment Period

3.6 years

First QC Date

May 20, 2025

Last Update Submit

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

Age18 Years - 65 Years
Sexfemale(Gender-based eligibility)
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Karolinska Institutet, Department of Dental Medicine

Stockholm, Huddinge, 14152, Sweden

Location

Biospecimen

Retention: SAMPLES WITH DNA

Saliva, blood

MeSH Terms

Conditions

Fibromyalgia

Condition Hierarchy (Ancestors)

Muscular DiseasesMusculoskeletal DiseasesRheumatic DiseasesNeuromuscular DiseasesNervous System Diseases

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

Locations