CBD oil put to the test for kids with Hard-to-Control seizures
NCT ID NCT07668856
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study is testing whether cannabidiol (CBD) oil can reduce seizures in children aged 1 to 18 with severe epilepsy that doesn't respond to standard treatments. Each child will receive both CBD and a placebo in alternating periods, and their seizures will be tracked using a smartphone app. The goal is to see if CBD works better than placebo for each individual child, while also monitoring safety and side effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cannabidiol (CBD) oral solution
- What this could lead to
- If it works, this could provide a personalized treatment option for children with hard-to-control epilepsy, reducing seizure frequency and improving quality of life.
- What could go wrong
- This is a small Phase 3 trial with only 50 participants, and results may not apply to all children. CBD may cause side effects like drowsiness or liver issues, and the benefit over placebo may be modest or absent for some.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Dec 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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1 year to 18 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Minimum age of 1 year old and maximum age of 18 years old. * Confirmed diagnosis of refractory epilepsy according to ILAE criteria * At least 4 countable seizures (not all in one week) of epileptic origin, during the 4-week baseline period while receiving care as usual. * All medication doses or other interventions for epilepsy must have been stable for one month prior to screening and the participants/parents and treating physicians are willing to maintain the current treatment regimen throughout the trial. * Informed consent/ of legal representative/ parents. * Presence of a consistently available patient caregiver for proxy-reports. Exclusion Criteria: * Any known or suspected hypersensitivity to cannabinoids or any of the excipients of the Investigational Medicinal Product (cannabis extract and refined peanut oil, generally safe for patients with peanut allergy) * History or current signs of significantly impaired liver function, such as bilirubin level ≥ 2 x upper limit of normal, or presence of liver damage as indicated by levels of alanine aminotransferase and/or aspartate aminotransferase ≥ 3 x upper limit. * Pregnancy, breastfeeding, or intention to become pregnant throughout the trial or within 3 months of completing treatment * Cardiac disease including: Structural heart disease with hemodynamic significance, heart failure, ischemic heart disease, Brugada syndrome, long-QT syndrome, cardiac arrythmia * Glaucoma * Ongoing evaluation for epilepsy surgery * Implementation of vagal nerve stimulation within 3 months prior to screening and unwillingness to delay inclusion until stable settings of vagal nerve stimulation are reached * Starting a ketogenic diet within 3 months prior to screening and unwillingness to delay inclusion until a stable ketogenic diet is reached * Unstable medical condition, other than refractory epilepsy, that is of significant influence on participation in the trial; significance to be determined with the treating physician/pediatric neurologist * History of recreational or medicinal cannabis use, or cannabinoid-based medications, within three months prior to screening and the patient is unwilling to abstain for the duration of the study * Planned intervention under general anesthesia interfering with the baseline period; or any planned major surgery within the duration of the trial * Expected inability to undergo blood sampling due to anxiety or resistance * Use of clobazam dosage of \> 0,5 mg/kg/day in the last month
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Medical Center Utrecht
RECRUITINGUtrecht, Utrecht, 3584 CX, Netherlands
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Reading the Brain's signals to predict who benefits from deep brain stimulation
- Can a Comfort-Focused education program improve life with epilepsy?
- Can video games rewire young brains after injury?
- High-Fat Diet's effect on epilepsy: scientists track brain signals
- Epilepsy drug candidate put to the test in healthy volunteers