EEG Dynamics in Lennox-Gastaut Syndrome Patients Undergoing Fenfluramine Treatment

Part of paid clinical trials in Chicago, Illinois.

Sponsor
University of Chicago
Study ID
NCT07555171
Status
Enrolling By Invitation

Conditions

  • Lennox Gastaut Syndrome (LGS)

Eligibility Criteria

Sex
ALL
Age
2 Years - 35 Years
Healthy Volunteers
Not accepted

Interventions

  • fenfluramine HCl — DRUG
    Patients who receive fenfluramine will be enrolled in this non-interventional study.

Study Details

This study plans to learn if certain markers found during electroencephalogram (EEG) analysis could predict fenfluramine responsiveness to give clinicians greater insight into the effectiveness of fenfluramine in people with Lennox Gastaut Syndrome (LGS).

Key Dates

Start date
Apr 30, 2026
Status verified
May 2026
Primary completion
Dec 31, 2027
Completion
Apr 30, 2028

Study Design

Enrollment
20 participants (estimated)

Primary Outcome Measure

Number of participants who have concordance between electroencephalogram (EEG) changes and clinical responsiveness in patients diagnosed with Lennox-Gastaut Syndrome (LGS) undergoing treatment with fenfluramine after 6 months. [ Time Frame: from EEG prior to fenfluarmine initiation to follow up EEG 6 months after ]

Locations (1)

FacilityCityStateZIPSite coordinators
University of ChicagoChicagoIllinois60637-

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