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Trial of Methyl B12 on Behavioral and Metabolic Measures in Children With Autism (B12)

Primary Purpose

Autistic Disorder

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Methyl B12
Placebo
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Autistic Disorder focused on measuring Autism, Pervasive Developmental Disorders

Eligibility Criteria

3 Years - 7 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of DSM IV defined autism and meets cut off on Autism Diagnostic Inventory-Revised (ADI-R) and/or the Autism Diagnostic Observation Scale (ADOS)
  • Age 3 through 7 years
  • IQ of 50 or above
  • Parental agreement to continue present dietary, behavioral or psychotropic drug treatment but not change treatment during 8 week intervention
  • Willingness to have blood drawn, without the use of a sedative prescription from the study doctor

Exclusion Criteria:

  • Bleeding disorder
  • Cancer
  • Seizure disorder
  • Fragile X or other known genetic cause of autism
  • Perinatal brain injury (i.e.: cerebral palsy)
  • Other serious medical illnesses
  • Current use of any B12 supplement

Sites / Locations

  • UCSF

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Active

Arm Description

Placebo

Active Methyl B12

Outcomes

Primary Outcome Measures

Clinical Global Impression-Improvement (CGI-I)
PI assesses subject's change using the CGI-I measure. This is a 7-point Likert scale that assesses improvement of the patient's condition. Scores range from the worst score of 7 (Very much worse) to the best score of 1 (Very much improved). Lower scores are better on this scale, and indicate greater improvement.

Secondary Outcome Measures

Full Information

First Posted
December 23, 2009
Last Updated
January 4, 2017
Sponsor
University of California, San Francisco
Collaborators
University of California, Davis, Arkansas Children's Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01039792
Brief Title
Trial of Methyl B12 on Behavioral and Metabolic Measures in Children With Autism
Acronym
B12
Official Title
Double Blind Placebo Controlled Trial of Methyl B12 on Behavioral and Metabolic Measures in Children With Autism
Study Type
Interventional

2. Study Status

Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
October 2013 (Actual)
Study Completion Date
November 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, San Francisco
Collaborators
University of California, Davis, Arkansas Children's Hospital Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether the supplement Methyl B12 is effective in treating some of the symptoms of Autism.
Detailed Description
Autism is a complex neurodevelopmental disorder with early childhood onset characterized by impairments in communication, social interaction, and repetitive behavior. Due to the lack of known treatments for autism, many parents seek complementary and alternative medical (CAM) therapies hoping to help their affected child. Methylcobalamin (methyl B12) is a commonly used CAM treatment that has anecdotal reports of remarkable clinical improvements with few side effects. Prior studies have found that children with autism have deficiencies in key metabolites and antioxidants which can be caused by methyl B12 deficiency; additional studies have shown that methyl B12 normalizes deficiencies in these metabolites and antioxidants. Based on these reports, a pilot study was conducted at UC Davis on the effect of methyl B12 on the behavioral and metabolic measures in children with autism. The preliminary results of 29 subjects revealed a subgroup of 9 responders to clinical behavior assessments. These responders also demonstrated significant improvement on the plasma measures of antioxidant capacity, suggesting methyl B12 improves symptoms in a subgroup of children with autism by increasing key antioxidants. The current study will have an 8 week double blind design with 50 subjects, designed to evaluate improvements from methyl B12 by using behavioral assessments and analysis of specific metabolites in the subjects' blood. This study will determine whether methyl B12 will lead to benefits in any of the core features of autism, and will examine metabolic changes with the hope of potentially identifying a biomarker for treatment response in a subgroup of subjects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Autistic Disorder
Keywords
Autism, Pervasive Developmental Disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
57 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Arm Title
Active
Arm Type
Experimental
Arm Description
Active Methyl B12
Intervention Type
Drug
Intervention Name(s)
Methyl B12
Other Intervention Name(s)
Vitamin B12, methylcobalamin
Intervention Description
75 µg/Kg subcutaneously injected once every 3 days
Intervention Type
Dietary Supplement
Intervention Name(s)
Placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Clinical Global Impression-Improvement (CGI-I)
Description
PI assesses subject's change using the CGI-I measure. This is a 7-point Likert scale that assesses improvement of the patient's condition. Scores range from the worst score of 7 (Very much worse) to the best score of 1 (Very much improved). Lower scores are better on this scale, and indicate greater improvement.
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
7 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of DSM IV defined autism and meets cut off on Autism Diagnostic Inventory-Revised (ADI-R) and/or the Autism Diagnostic Observation Scale (ADOS) Age 3 through 7 years IQ of 50 or above Parental agreement to continue present dietary, behavioral or psychotropic drug treatment but not change treatment during 8 week intervention Willingness to have blood drawn, without the use of a sedative prescription from the study doctor Exclusion Criteria: Bleeding disorder Cancer Seizure disorder Fragile X or other known genetic cause of autism Perinatal brain injury (i.e.: cerebral palsy) Other serious medical illnesses Current use of any B12 supplement
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert L. Hendren, DO
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
UCSF
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26889605
Citation
Hendren RL, James SJ, Widjaja F, Lawton B, Rosenblatt A, Bent S. Randomized, Placebo-Controlled Trial of Methyl B12 for Children with Autism. J Child Adolesc Psychopharmacol. 2016 Nov;26(9):774-783. doi: 10.1089/cap.2015.0159. Epub 2016 Feb 18.
Results Reference
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Trial of Methyl B12 on Behavioral and Metabolic Measures in Children With Autism

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