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Canabidiol (CBD) for Treatment of Frontal Lobe Epilepsy

Efficacy of Cannabidiol (CBD) in Patients with Treatment-Resistant Frontal Lobe Epilepsy

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210608051515N1
Enrollment
30
Registered
2021-06-12
Start date
2021-07-21
Completion date
Unknown
Last updated
2021-06-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Treatment Resistant Epilepsy. Epilepsy and recurrent seizures

Interventions

Intervention 1: Intervention group: Patients diagnosed with frontal lobe epilepsy who are resistant to common drug therapies. These patients are randomly assigned to the intervention group according t

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Drug resistant frontal lobe epilepsy diagnosis (Insufficient or no response to two or more of anti epileptic agents)

Exclusion criteria

Exclusion criteria: Consumption of any derivative of marijuana or cannabis plant in recent month Pregnancy Any of the aforementioned medications in regimen: Clobazam, DesMethyl Clobazam, Eslicarbazepin, Topiramate, Zonisamide, Warfarin

Design outcomes

Primary

MeasureTime frame
Decrease in the seizure frequency in drug-resistant frontal lobe epilepsy following cannabidiol use. Timepoint: Before the intervention and after 14 weeks of taking the drug or placebo. Method of measurement: Based on the patient's history and counting the number of seizures per month.

Secondary

MeasureTime frame
Decrease in the severity of seizures after taking cannabidiol according to the Chalfont seizure severity scale. Timepoint: Before the intervention and after fourteen weeks of taking drug or placebo. Method of measurement: Based on the Chalfont seizure severity by scoring system.;Increase in quality of life in epilepsy following cannabidiol use. Timepoint: Before the intervention and after the fourteen weeks of taking medication or placebo. Method of measurement: Quality of Life in Epilepsy with 31 questions (QOLIE-31) questionnaire by scoring.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeyyed Reza Ebadi

Tehran University of Medical Sciences

seyyedrezae@gmail.com+98 21 8821 2409

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 9, 2026