Efficacy Study of Subcutaneous Methyl-B12 in Children With Autism
Autistic Disorder
About this trial
This is an interventional treatment trial for Autistic Disorder focused on measuring Autism, Placebo, B12, Controlled, Complementary Alternative Medicine, Vitamin Supplement
Eligibility Criteria
Inclusion Criteria: Diagnosis of DSM IV defined autism and meets cut off on Autism Diagnostic Inventory-Revised (ADI-R) and the Autism Diagnostic Observation Scale (ADOS). Age 3 to 8 years IQ of 50 or above Willingness of parents to administer subcutaneous methyl B12. Parental agreement to continue present dietary, behavioral or psychotropic drug treatment but not change treatment during 12 week intervention or wait list. Exclusion Criteria: Clinical evidence of seizure disorder Cancer Recent surgery Active infection with fever Fragile X or other known genetic cause of autism Bleeding disorder Perinatal brain injury (e.g. cerebral palsy) Current use of any methyl B12 product Evidence for malnutrition seen in abnormal albumin level
Sites / Locations
- UC Davis MIND Institute
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
A
B
Methyl-B12
Saline placebo