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Vitamin/Mineral Supplement for Children and Adults With Autism

Autism Clinical Trial

Official title:
New Vitamin/Mineral Supplement for Children and Adults With Autism - National Study

Clinical Trial Summary

The investigators hypothesis is that a new, revised formulation of a vitamin/mineral supplement will result in:

1. improvement of nutritional status in some children/adults with autism, and

2. reduction of some of the symptoms of autism in some children

Clinical Trial Description

The major goal of this study is to determine the effect of this vitamin/mineral supplement on levels of vitamins, minerals, neurotransmitters, and biomarkers for nutritional deficiencies. The study design is a randomized, double-blind, placebo-controlled. Blood and urine measurements will be measured at the beginning of the study in children with autism and typical children. Then, the children with autism will be given the supplement or placebo for 12 weeks, and then their blood and urine will be re-measured. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01225198
Study type Interventional
Source Arizona State University
Contact
Status Completed
Phase Phase 2
Start date May 2008
Completion date February 2009
View Details
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