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Atkins Diet for Difficult-to-Control Headaches in Teenagers
This study is currently recruiting participants.
Verified by Johns Hopkins University, May 2008
Sponsored by: Johns Hopkins University
Information provided by: Johns Hopkins University
ClinicalTrials.gov Identifier: NCT00181064
  Purpose

This is a 3-month pilot study of 10 adolescents with chronic daily headache. Teens will be placed on a modified Atkins diet and followed with 2 subsequent visits to assess for headache improvement.


Condition Intervention Phase
Chronic Daily Headache
Behavioral: Modified Atkins diet
Phase I

MedlinePlus related topics: Headache
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety/Efficacy Study
Official Title: Use of the Atkins Diet for Adolescents With Chronic Daily Headache.

Further study details as provided by Johns Hopkins University:

Primary Outcome Measures:
  • Headaches [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Ketosis [ Time Frame: 3 months ] [ Designated as safety issue: No ]
  • Diet duration [ Time Frame: as long as tolerated ] [ Designated as safety issue: No ]
  • Quality of life (PedsMIDAS) [ Time Frame: 3 months ] [ Designated as safety issue: No ]

Estimated Enrollment: 10
Study Start Date: September 2005
Estimated Study Completion Date: July 2009
Estimated Primary Completion Date: June 2009 (Final data collection date for primary outcome measure)
Intervention Details:
    Behavioral: Modified Atkins diet
    15 grams of carbohydrates per day - high fat diet
Detailed Description:

Patients are placed on the diet and followed with various measures for 3 months. If the diet is helpful it is continued. Patients are still being enrolled as of 9/6/06.

  Eligibility

Ages Eligible for Study:   12 Years to 19 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Ages 12-19
  • Minimum 15 headaches/month for at least 3 months
  • Tried 2 preventative medications previously

Exclusion Criteria:

  • Prior use of the Atkins diet for more than 1 week
  • Pregnancy
  • Significant heart or kidney disease
  • Dangerously underweight
  • Using acute pain medications more than 11 days in the past month
  • Medications being changed
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00181064

Contacts
Contact: Eric H Kossoff, MD 410-614-6054 ekossoff@jhmi.edu
Contact: Jennifer Huffman, MD 410-502-8073 jhuffma2@jhmi.edu

Locations
United States, Maryland
Johns Hopkins Hospital Recruiting
Baltimore, Maryland, United States, 21287
Contact: Eric H. Kossoff, MD     410-614-6054     ekossoff@jhmi.edu    
Principal Investigator: Eric H Kossoff, MD            
Sub-Investigator: Jennifer Huffman, MD            
Sub-Investigator: Jack Gladstein, MD            
Sponsors and Collaborators
Johns Hopkins University
Investigators
Principal Investigator: Eric H Kossoff, MD Johns Hopkins University
  More Information

Publications:
Responsible Party: Johns Hopkins University ( Eric Kossoff )
Study ID Numbers: 05-08-10-04
Study First Received: September 9, 2005
Last Updated: May 7, 2008
ClinicalTrials.gov Identifier: NCT00181064  
Health Authority: United States: Institutional Review Board

Keywords provided by Johns Hopkins University:
headache
Atkins
ketosis
intractable

Study placed in the following topic categories:
Signs and Symptoms
Headache
Central Nervous System Diseases
Neurologic Manifestations
Pain
Brain Diseases
Ketosis
Headache Disorders

Additional relevant MeSH terms:
Nervous System Diseases

ClinicalTrials.gov processed this record on January 16, 2009