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 — DRUGPatients 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)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Chicago | Chicago | Illinois | 60637 | - |
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