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临床试验/NCT01039792
NCT01039792已完成2 期

Double Blind Placebo Controlled Trial of Methyl B12 on Behavioral and Metabolic Measures in Children With Autism

University of California, San Francisco1 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
57
试验地点
1
主要终点
Clinical Global Impression-Improvement (CGI-I)

研究概览

简要总结

The purpose of this study is to determine whether the supplement Methyl B12 is effective in treating some of the symptoms of Autism.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
3 Years 至 7 Years(Child)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • Bleeding disorder
  • 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

研究组 & 干预措施

Placebo

Placebo Comparator

Placebo

干预措施: Placebo (Dietary Supplement)

Active

Experimental

Active Methyl B12

干预措施: Methyl B12 (Drug)

结局指标

主要结局

Clinical Global Impression-Improvement (CGI-I)

时间窗: 8 weeks

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.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Robert Hendren

Professor of Psychiatry, Director of Child & Adolescent Psychiatry

University of California, San Francisco

研究点 (1)

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