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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02216500
Other study ID # IRB201500942
Secondary ID OCR25124
Status Recruiting
Phase N/A
First received
Last updated
Start date September 2006
Est. completion date October 2031

Study information

Verified date May 2024
Source University of Florida
Contact Peggy R. Borum, Ph.D.
Phone 352-562-2861
Email prb@ufl.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Approximately a fourth of children with seizures do not respond adequately to available therapy. Ketogenic therapy has a long history as treatment for intractable epilepsy, but there is no agreement concerning how it works and what is the best way to administer it. This natural history study will collect data pertaining to both questions.


Description:

The basis of Ketogenic Therapy is an altered macronutrient intake. It is based on a ratio of fat: protein+carbohydrate in which protein intake is adequate and carbohydrate is minimal. On Ketogenic Therapy, the body metabolizes fat, producing ketones as an energy source for the brain. Induction of ketosis has been shown to correlate with the reduction of seizures observed with Ketogenic Therapy. A major challenge of Ketogenic Therapy in children is that the compounds provided to stop seizure activity are the same compounds provided for growth and development. The altered macronutrient ratio that is the basis of Ketogenic Therapy is also a potential risk factor for dyslipidemia and may adversely affect growth. The investigators will evaluate efficacy of Ketogenic Therapy by assessing seizures and requirements for antiepileptic drugs. The investigators will evaluate adverse effects of Ketogenic Therapy by assessing dyslipidemia and growth. The investigators will foster optimal daily administration of therapy with structured training programs for caregivers.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date October 2031
Est. primary completion date October 2030
Accepts healthy volunteers No
Gender All
Age group N/A to 50 Years
Eligibility Inclusion Criteria: - Patients whose physician has prescribed the ketogenic diet - Patients with lab tests consistent with the ability to metabolize a high fat and low carbohydrate diet - Patients that can be compliant with administration of the therapy and with record keeping. Exclusion Criteria: - Patients with lab tests consistent with the inability to metabolize a high fat and low carbohydrate diet - Patients at risk of being non-compliant with administration of the therapy and with record keeping

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Ketogenic Therapy
Ketogenic Therapy is based on a ratio of fat: protein+carbohydrate in which protein intake is adequate, fat intake is high, and carbohydrate intake is minimal.

Locations

Country Name City State
United States University of Florida Gainesville Florida

Sponsors (1)

Lead Sponsor Collaborator
University of Florida

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reduced seizures Seizures will be charted from collected data. 2 years
Secondary Reduced requirement for medications Medication will be charted from collected data. 2 years
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