Forty-five subjects receiving no dietary therapy with a proven G1D diagnosis will be enrolled. To evaluate the effect of C7 supplementation of a regular diet on a EEG activity in addition to IQ, language, working memory, processing speed, emotional and behavioral functioning, ataxia, and other neuropsychological and neurological performance indices in children and adults genetically diagnosed with G1D receiving a regular diet at enrollment.
Age range
24 Months – 35 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Neuropsychological Score of Sustained Attention
Timeframe: Change post 6 months of treatment
Neuropsychological Score of Sustained Attention
Timeframe: Change after 3 months off treatment
Neuropsychological Score of Working Memory Index Scale (WMI)
Timeframe: Change post 6 months of treatment
Neuropsychological Score of Working Memory Index Scale (WMI)
Timeframe: Change after 3 months off-treatment
Neuropsychological Score of Processing Speed Index (PSI)
Timeframe: Change post 6 months of treatment
Neuropsychological Score of Processing Speed Index (PSI)
Timeframe: Change after 3 months off-treatment