Anxiety Clinical Trial - Epidiolex® for Anxiety in Pediatric Epilepsy

Status Recruiting

Clinical Trial Summary

This is a prospective open label study assessing the efficacy and tolerability of pharmaceutical grade cannabidiol--Epidiolex (R), for the treatment of anxiety in pediatric patients with pediatric epilepsy that has been difficult to treat and requires ongoing use of anticonvulsant medication.

Clinical Trial Description

This study is an open label, adjunctive, proof of concept clinical trial. Prospective participants will be considered for the study if neurologic status suggests the need for continued treatment, and behavioral characteristics are clinically significant. All participants will receive active treatment, involving flexible dose titration of Epidiolex® and will be monitored for a period of four months. The study will be monitored and overseen by the Johns Hopkins Hospital Institutional Review Board. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05324449
Study type	Interventional
Source	Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Contact	Catherine Eliades
Phone	443-923-3824
Email	eliades@kennedykrieger.org
Status	Recruiting
Phase	Phase 4
Start date	April 5, 2022
Completion date	April 4, 2026

View Details

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