Clinical Trial

Evaluation of Efficacy and Safety of Topical Cannabidiol (Canvert-M Produced by Alasht Pharmed co. Iran) in the Treatment of Migraine Attacks

Recruiting Phase 4
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Record status
This record was last updated July 30, 2025 (before its estimated September 16, 2025 completion). Its status may not reflect the trial's current state.
Summary
Canvert-M (manufactured by Alasht Pharmed Co. Iran) is a topical roll-on formulation that contains cannabidiol, peppermint, lavender, rosemary, eucalyptus, wintergreen, basil oil, etc. This phase IV, single-arm, open-label clinical trial evaluated the efficacy and safety of Canvert-M in males and females aged 18 to 55 years diagnosed with migraine according to the International Classification of Headache Disorders, 3rd edition (ICHD-3), for the treatment of migraine attacks. The primary objective was to assess the reduction in headache intensity using a 4-point scale (0=no headache, 1=mild headache, 2=moderate headache, 3=severe headache). Secondary objectives included evaluating additional efficacy and safety outcomes of Canvert-M in managing migraine attacks.
Trial Details
NCT Number NCT07093138
Lead Sponsor Alasht Pharmed
Conditions Migraine Disorders
Enrollment 30 participants
Start Date 2025-07-16
Primary Completion 2025-09-16 (estimated)
Study Completion 2025-09-16 (estimated)
Updated on ClinicalTrials.gov 2025-07-30