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Clinical Trials in Poland / NCT06405646
Enrolling by invitation Observational

Concentration of Receptors With Affinity for Cannabidiol and Cannabinol and the Effect on Chronic Orofacial Pain of Muscle Origin

NCT06405646 · tracked via the Priya Life Science Poland tracker
Phase
Observational
Started
2025-04-01
Last updated
2026-03-06

Condition(s) studied

MyalgiaMuscle PainOrofacial PainHeadache, TensionHeadaches Muscular

Investigational drug(s) / intervention(s)

Blood CB1, CB2, TRPV-1 concentration measurement

Blood CB1, CB2, TRPV-1 concentration measurement: In each of the patients blood CB1, CB2, TRPV-1 concentration will be measure

Study summary

The main aim of the presented project will be to examine the concentration of selected receptors (CB1, CB2, TRPV-1) showing affinity for binding to cannabidol (CBD) and cannabinol (CBN) in blood samples collected from people with chronic pain in the masticatory muscles and from people without this pain. Moreover, study participants will be examined by a qualified doctor, according to the validated and standardized international DC/TMD protocol (Diagnostic Criteria for Temporomandibular Disorders) and the criteria included in ICOP-1 (International Classification of Orofacial Pain, 1st edition). The nature and duration of pain, psychoemotional state and central sensitization (the phenomenon of increased reactivity of the nervous system to stimuli) will be determined using validated questionnaires. The obtained results will be subjected to statistical analysis in order to check the relationships between the examined parameters.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: * age over 18, under 80 * the presence of chronic pain in the muscles of the masticatory system, which lasts for more than 3 months in accordance with the international criteria included in ICOP-1. Exclusion Criteria: * people under 18 years of age * pregnant or breastfeeding women, * obese people, * people with active cancer, * people with severe systemic diseases, including genetic and neurological diseases, * people with severe mental illnesses and taking psychoactive substances, people who are taking or have taken antidepressants and/or myorelaxants and/or other drugs that affect neuromuscular activity in the last 12 months * people addicted to alcohol, drugs and other psychoactive substances * condition after craniofacial injuries

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Wroclaw Medical University Wroclaw Poland

More Wroclaw Medical University trials in Poland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06405646 on ClinicalTrials.gov ↗ ← All trials in Poland