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Набор по приглашению NCT05961501

The Effectiveness of CBD and CBN in the Treatment of Facial Pain and Headache of Muscular Origin

Фаза II / Фаза III С лечением Myalgia Muscle Pain Orofacial Pain Headache, Tension

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: An aqueous solution containing CBD and CBN, The aqueous solution of placebo.
Кому может быть актуально
Состояния в реестре: Myalgia, Muscle Pain, Orofacial Pain, Headache, Tension. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Польша
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

The Evaluation of the Effectiveness of Cannabidiol (CBD) and Cannabinol (CBN) Oral Solutions in the Treatment of Facial Pain and Headache of Muscular Origin

Обзор

The aim of the study is to evaluate the effectiveness of an aqueous solution containing CBD and CBN in the management of Facial Pain and Headache of Muscular Origin. A randomized (block randomization), double-blind, two-arm controlled trial will involve 42 adult patients diagnosed with Facial Pain and Headache of Muscular Origin which is lasting more than 3 months on the basis of clinical examination. Qualified study participants will be randomly assigned to two groups. The studied group will receive tan aqueous solution containing CBD and CBN, to drink at home in the dose determined by the attending physician, while the control group will receive an aqueous solution of placebo, to drink at home in the dose determined by the attending physician during this time. Each subject will be tested on the qualification day (D0), on 20 days after D0 (D20), and then 40 (D40) and 60 (D60) days after the qualification day using electromyography (EMG), pressure pain threshold test (PPT), clinical examination and surveys.

Подробное описание

Background: Orofacial pain is a common occurrence. According to available scientific research, it occurs in up to 16 to 25% of the human population. In its chronic form, orofacial pain can lead to reduced sleep quality, reduced life satisfaction, and psychoemotional disorders, including depressive disorders. A popular tendency among patients suffering from chronic orofacial pain is the abuse of non-steroidal anti-inflammatory drugs, which in most cases show low, short-term and disproportionate to side effects effectiveness. There are scientific reports suggesting that substances such as cannabidiol (CBD) and cannabinol (CBN) may be effective in the treatment of chronic nociceptive and neuropathic pain. However, studies on the effectiveness of these substances in alleviating muscular orofacial pain are clearly lacking

Aim: The aim of the study is to evaluate the effectiveness of an aqueous solution containing CBD and CBN in the management of Facial Pain and Headache of Muscular Origin

Material and methods: A randomized (block randomization), double-blind, two-arm controlled trial will involve 42 adult patients diagnosed with Facial Pain and Headache of Muscular Origin which is lasting more than 3 months on the basis of clinical examination. Criteria for exclusion from the study will include: patients under 18 years of age, patients who are allergic to any ingredient of the preparation, pregnant or breast-feeding women, patients taking preparations that contain similar ingredients and/or have similar effects, obese patients, patients with active cancer, patients with severe systemic diseases, including genetic and neurological diseases, patients with severe mental illnesses, patients who are taking or in the last 12 months have taken antidepressants and/or myorelaxants and/or other drugs that affect neuromuscular activity, patients addicted to alcohol or drugs.

Qualified study participants will be randomly assigned to two groups. The studied group will receive an aqueous solution containing CBD and CBN, to drink at home in the dose determined by the attending physician, while the control group will receive an aqueous solution of placebo, to drink at home in the dose determined by the attending physician during this time. Each subject will be tested on the day of qualification (day 0), after 20 (day 20), and then 40 (day 40) and 60(day 60) days after the qualification day using the following methods:

* EMG (Electromyography) (day 0, day 20, day 40, day 60) * Pressure pain threshold test (PPT) using the Wagner Paintest FPX 25 algometer (day 0, day 20, day 40, day 60) * Clinical examination according to diagnostic criteria for temporomandibular disorders - DC / TMD International Examination Form (day 0, day 20, day 40, day 60) * Surveys: Graded Chronic Pain Scale oraz McGill Pain Questionnaire (day 0, day 20, day 40, day 60), Satisfaction with Life Scale (day 0, day 20, day 40, day 60), Pittsburgh Sleep Quality Index (day 0, day 20, day 40, day 60), The Migraine Disability Assessment Test -MIDAS (day 0, day 20, day 40, day 60), Central Sensitisation Inventory (CSI) (day 0, day 20, day 40, day 60), Bruxscreen Q (day 0, day 20, day 40, day 60), Generalised Anxiety Disorder Assessment (day 0, day 20, day 40, day 60), Insomnia Severity Index (day 0, day 20, day 40, day 60), The Perceived Stress Scale (day 0, day 20, day 40, day 60), Somatic Symptom Scale - 8 (day 0, day 20, day 40, day 60)

Вмешательства

  • Препарат An aqueous solution containing CBD and CBN
    An aqueous solution containing CBD and CBN, to drink at home in the dose determined by the attending physician
  • Другое The aqueous solution of placebo
    An aqueous solution of placebo, to drink at home in the dose determined by the attending physician

Первичные конечные точки

  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed using pressure pain threshold test (PPT) using the Wagner Paintest FPX 25 algometer. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on electrical activity and nerve conduction in muscles using EMG ( Electromyography). [Срок оценки: 3 months]
Вторичные конечные точки (12)
  • The effectiveness of an aqueous solution containing CBD and CBN reduction on Facial Pain and Headache of Muscular Origin assessed by clinical examination in accordance to Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) protocol. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on reduction of Facial Pain and Headache of Muscular Origin using Pain Numerical Rating Scale. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed using Graded Chronic Pain Scale. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed using McGill Pain Questionnaire. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed using Pittsburgh Sleep Quality Index. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed using Satisfaction with Life Scale Questionnaire. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed using the Migraine Disability Assessment Test - MIDAS [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed by Central Sensitization Inventory [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed by Bruxscreen Q questionnaire. [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed by Generalized Anxiety Disorder -7 [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed by Insomnia Severity Index (ISI) [Срок оценки: 3 months]
  • The influence of an aqueous solution containing CBD and CBN on muscle pain assessed by Perceived Stress Scale -10 [Срок оценки: 3 months]

Критерии участия

Критерии включения

  • facial pain and headache of muscular origin for more than 3 months

Критерии исключения

  • patients under 18 years of age,
  • patients who are allergic to any ingredient of the preparation,
  • pregnant or breast-feeding women,
  • patients taking preparations that contain similar ingredients and/or have similar effects,
  • obese patients,
  • patients with active cancer,
  • patients with severe systemic diseases, including genetic and neurological diseases,
  • patients with severe mental illnesses,
  • patients who are taking or in the last 12 months have taken antidepressants and/or myorelaxants and/or other drugs that affect neuromuscular activity,
  • patients addicted to alcohol or drugs.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Тройное слепое
Основная цель
Лечение

Центры проведения

Польша · 1 центр
  • Wroclaw Medical University — Wroclaw

Идентификаторы

NCT: NCT05961501 · WMU1/2023

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗