Clin2
NCT06924827Possibly a fitNot yet recruiting

Switching children from artisanal CBD to Epidiolex

Dravet Syndrome (DS)Lennox-Gastaut Syndrome (LGS)

Treatments studied

Part of Brain & nervous system, Genetic & congenital clinical trials.

This study looks at switching children with Dravet or Lennox Gastaut syndrome from artisanal CBD products to a standardized FDA-approved CBD medication called Epidiolex, to see if it works as well or better for seizure control.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
25 people
Ages
2 years to 18 years
Study type
Interventional

Who can take part

  • Children aged 2 to 18 years old with Dravet or Lennox Gastaut syndrome.
  • Must be currently taking a stable dose of artisanal CBD (with a high CBD to THC ratio) for at least 3 months.
  • Must also be taking at least one other seizure medication, stable for at least 28 days.
  • If using a vagal nerve stimulator or ketogenic diet, the settings must be stable.
  • Must be willing to keep a seizure diary and avoid other cannabis products or alcohol during the study.
  • Cannot have used Epidiolex before, or be pregnant, breastfeeding, or have certain liver problems.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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