Use of the Atkins Diet for Children With Sturge Weber Syndrome

Epilepsy Clinical Trial

Official title:

Use of the Atkins Diet for Children With Sturge Weber Syndrome

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00639730
• Other study ID #: NA_00003359
• Status: Completed
• Phase: Phase 1
• First received: March 14, 2008
• Last updated: May 26, 2010
• Start date: May 2006
• Est. completion date: May 2010

Study information

• Verified date: May 2010
• Source: Johns Hopkins University
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

This research is being done to find out if the Atkins Diet can be used safely and effectively to reduce seizures in children who have Sturge Weber syndrome.

The ketogenic diet is a proven therapy for epilepsy, but can be difficult to use in children. The Atkins Diet is a high fat, high protein, low carbohydrate diet introduced in the 1970s to help with weight loss. It is different from the ketogenic diet in four major ways: no calorie restriction, no fluid restriction, no protein restriction, and is easy to start outside the hospital. People on the Atkins Diet become ketotic (produce high levels of ketones, a certain substance in the body), like patients on the ketogenic diet, and the investigators believe this may lead to seizure control.

Children aged 2-18 with Sturge Weber syndrome and seizures at least monthly, who have used at least two anti-seizure drugs may join. 5 children in total will be enrolled.

Description:

If you agree to be in this study, we will ask you to do the following things:

Before the diet is started:

• We will ask you to keep track of your child's seizures daily for 2 weeks before starting the Atkins diet and provide us with a 3-day food record as well.

• Baseline blood (about 2 teaspoons) and urine work will be obtained.

• We will give you a free copy of a carbohydrate-counting guide.

• You will be asked to fill out a 3-day food record.

On the diet:

• Give your child a daily calcium supplement and multivitamin.

• Keep a daily seizure log.

• Check urine for ketones (to make sure the diet is working) and specific gravity (to make sure your child is well hydrated) twice a week and when you come to clinic.

• We will ask you to weigh your child at home every week, and we will weigh him or her when you come into clinic too.

• Do not fluid restrict your child; please give plenty of carbohydrate-free fluids.

• You will give 20 grams per day of carbohydrates. We will give you instructions on how to measure daily intake of carbohydrates.

• We will not change medications for the first three months. Do not change your child's seizure medicines without checking with our doctors.

• For the first three months, we ask you to avoid store-bought low-carbohydrate products (as they can have more carbohydrates than advertised).

After being on the diet for one month, Dr. Kossoff will contact you by telephone to discuss how your child is doing. You can also speak with one of our dietitians. We will discuss the 3-day food record with you

You will be asked to come to the clinic (outpatient center, 5th floor) for two follow-up visits:

1. after being on the diet for 3 months and

2. after being on the diet for 6 months.

During these visits you will meet with one of our doctors and a dietitian. We will review your child's seizure control and health. We may obtain blood (about 2 teaspoons). We will check your child's urine for ketones and specific gravity.

If the diet is helping beyond 6 months, we will help your child continue on the diet with clinic visits and labs as necessary, at a carbohydrate amount that is most helpful.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 5
• Est. completion date: May 2010
• Est. primary completion date: March 2010
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 2 Years to 18 Years

Eligibility

Inclusion Criteria:

• 2-18 years

• Sturge Weber syndrome

• Monthly seizures (at least)

• Tried at least two anticonvulsants

Exclusion Criteria:

• Prior use of the Atkins or ketogenic diets

• Patients with non-epileptic seizures (pseudoseizures) will be excluded

• Patients that are pregnant or become pregnant during the study will be excluded

• High cholesterol

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Brain Stem Infarctions
• Epilepsy
• Sturge Weber Syndrome
• Sturge-Weber Syndrome
• Syndrome

Intervention

Dietary Supplement:
• modified Atkins diet
High fat, low carbohydrate diet

Locations

Country	Name	City	State
United States	Johns Hopkins Hospital	Baltimore	Maryland

Sponsors (2)

Lead Sponsor	Collaborator
Johns Hopkins University	Vascular Birthmarks Foundation

Country where clinical trial is conducted

United States, 

References & Publications (2)

Kossoff EH, McGrogan JR, Bluml RM, Pillas DJ, Rubenstein JE, Vining EP. A modified Atkins diet is effective for the treatment of intractable pediatric epilepsy. Epilepsia. 2006 Feb;47(2):421-4. — View Citation

Kossoff EH, Turner Z, Bluml RM, Pyzik PL, Vining EP. A randomized, crossover comparison of daily carbohydrate limits using the modified Atkins diet. Epilepsy Behav. 2007 May;10(3):432-6. Epub 2007 Feb 26. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Seizures	Seizure frequency will be compared to baseline (pre-Diet).	6 months	No
Secondary	Ketosis		6 months	No
Secondary	Safety (stroke like events)		6 months	Yes