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ENROLLING BY INVITATION
NCT05961501
PHASE2/PHASE3

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

Sponsor: Wroclaw Medical University

View on ClinicalTrials.gov

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

DRUG

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

OTHER

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