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A Trial of CM-AT in Children With Autism - NCT00881452-32763(Clinical Trial 364649)



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City:  Orange City
State:  
FL
Zip Code: 32763
Conditions: Autism
Purpose: The purpose of this study is to determine whether CM-AT is safe and effective in treating the core symptoms of autism.
Study summary: Autism is currently a significant cause of disability in the pediatric population. Treatment is based upon the observation that many children with autism do not digest protein. CM-AT is a proprietary enzyme that is designed as a powder taken three times a day.
Criteria: Inclusion Criteria: - Meets the current Diagnostic and Statistical Manual for Mental Disorders (DSM-IV-TR) diagnostic criteria for autistic disorder (AD) Exclusion Criteria: - Patient weighing < 11kg (24.2 lbs.) - Demonstrated previous allergy to porcine (pork) products - Previous history of severe head trauma or stroke, seizure within one year of entering study or uncontrolled systemic disease - Diagnosis of: HIV, cerebral palsy, endocrine disorder, pancreatic disease - Within 30 days of starting the study, certain supplementation, chelation or dietary restriction (a 30 day washout period would be required for inclusion) - Use of of any stimulant medication must be discontinued 5 days prior to entering the study. - Subject must have a stable dose of SSRI's for at least 30 days.
Study is available at: Lake Mary Pediatrics
Orange City, FL 32763
United States

Primary Contact:
Heidi Anderson, RN
Email: cclinical2@aol.com
Phone: 386-960-8282

Secondary Contact:
Kristin Walsh, RN MSN
Email: kristin.walsh@curemark.com
Phone: 914-925-3697
If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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Data Source: ClinicalTrials.gov
Date Processed: March 23, 2011
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