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A multicenter study of the efficacy of the ketogenic diet
E P Vining1, J M Freeman, K Ballaban-Gil
1The Johns Hopkins Medical Institutions, Baltimore, MD 21287-7247, USA.
Insights
The ketogenic diet significantly reduced seizures in children with intractable epilepsy. This dietary therapy proved effective across multiple clinical settings, offering a viable treatment option.
Area of Science:
- Neurology
- Pediatric Epilepsy
- Nutritional Therapy
Background:
- Intractable epilepsy in children poses significant management challenges.
- The ketogenic diet is a high-fat, adequate-protein, low-carbohydrate diet used therapeutically.
Purpose of the Study:
- To evaluate the efficacy of the ketogenic diet in a multi-center study.
- To assess seizure frequency reduction in pediatric patients with intractable epilepsy.
Main Methods:
- Prospective study involving 51 children (aged 1-8 years) with intractable seizures.
- Ketogenic diet initiated after hospitalization and fasting, followed for at least 6 months.
- Seizure frequency monitored via parental calendars, compared to baseline at 3, 6, and 12 months.
Main Results:
- At 6 months, 55% of children experienced at least a 50% decrease in seizure frequency.
- At 1 year, 40% showed over a 50% seizure reduction, with 10% seizure-free.
- Diet adherence was 88% at 3 months, decreasing to 47% at 1 year.
Conclusions:
- The ketogenic diet is an effective intervention for reducing seizures in children with difficult-to-control epilepsy.
- The diet can be successfully implemented in diverse clinical environments.
- Treatment outcomes were not significantly influenced by patient demographics or EEG findings.
Objective:
To determine the efficacy of the ketogenic diet in multiple centers.
Design:
A prospective study of the change in frequency of seizures in 51 children with intractable seizures who were treated with the ketogenic diet.
Setting:
Patients were enrolled from the clinical practices of 7 sites. The diet was initiated in-hospital and the patients were followed up for at least 6 months.
Patients:
Fifty-one children, aged 1 to 8 years, with more than 10 seizures per week, whose electroencephalogram showed generalized epileptiform abnormalities or multifocal spikes, and who had failed results when taking at least 2 appropriate anti-epileptic drugs.
Intervention:
The children were hospitalized, fasted, and a 4:1 ketogenic diet was initiated and maintained.
Main Outcome Measures:
Frequency of seizures was documented from parental calendars and efficacy was compared with prediet baseline after 3, 6, and 12 months. The children were categorized as free of seizures, greater than 90% reduction, 50% to 90% reduction, or lower than 50% reduction in frequency of seizures.
Results:
Eighty-eight percent of all children initiating the diet remained on it at 3 months, 69% remained on it at 6 months, and 47% remained on it at 1 year. Three months after initiating the diet, frequency of seizures was decreased to greater than 50% in 54%. At 6 months, 28 (55%) of the 51 initiating the diet had at least a 50% decrease from baseline, and at 1 year, 40% of those starting the diet had a greater than 50% decrease in seizures. Five patients (10%) were free of seizures at 1 year. Age, sex, principal seizure type, and electroencephalogram were not statistically related to outcome.
Conclusion:
The ketogenic diet is effective in substantially decreasing difficult-to-control seizures and can successfully be administered in a wide variety of settings.
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