About this trial
To assess clinical outcomes in drug resistant epileptic pediatric patient by modified atkin diet with focusing on following points:
1. Control of seizures(frequency , duration and numbers of hospital admissions) . 2. Quality of life by pediatric quality of life inventory v4. 3. Cognitive function by stanford binet intelligence scale 5th edition. 4. Growth parameters ( weight, height will be combined to report BMI in kg/m\^2).
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Children aged 1-18 years.
Diagnosed with drug-resistant epilepsy according to ILAE definition.[2]
On KD for at least 6 months.
Disqualifiers
- Patients with contraindicated metabolic/genetic conditions.
Non-compliance with KD .
Trial population
This study will include pediatric patients with drug-resistant epilepsy (DRE) attending the ketogenic diet clinic at the Pediatric Neurology Unit, Sohag University Hospital. Eligible participants are children aged 1-18 years who meet the International League Against Epilepsy (ILAE) definition of DRE and have been on a ketogenic dietary therapy, specifically the Modified Atkins Diet (MAD), for at least 6 months.
Trial design
Case-only
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
1-Control of seizures(frequency and duration of seizures) . 2-Quality of life by pediatric quality of life inventory v4. 3-Cognitive function by stanford binet intelligence scale 5th edition. 4-Growth parameters (weight and height by BMI in kg/m^2)
Secondary outcomes
to detect clinical predictors of seizures control ( frequency of attack and duration) in patients with drug resistant epilepsy using MAD.
Sponsors and contacts
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