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The Effectiveness of CBD and CBN in the Treatment of Facial Pain and Headache of Muscular Origin
Sponsor: Wroclaw Medical University
Summary
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.
Official title: The Evaluation of the Effectiveness of Cannabidiol (CBD) and Cannabinol (CBN) Oral Solutions in the Treatment of Facial Pain and Headache of Muscular Origin
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
42
Start Date
2025-04-01
Completion Date
2026-12
Last Updated
2026-03-06
Healthy Volunteers
No
Interventions
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
The aqueous solution of placebo
An aqueous solution of placebo, to drink at home in the dose determined by the attending physician
Locations (1)
Wroclaw Medical University
Wroclaw, Poland