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Omega 3 Fatty Acids in the Treatment of Children With Autism Spectrum Disorders

U

University of Medicine and Dentistry of New Jersey

Status

Completed

Conditions

Autism

Treatments

Other: Placebo
Drug: Omega 3 fatty acids

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT00467818
0220060238
5R21AT002927 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Published studies on omega 3 fatty acids in the treatment of bipolar disorder and schizophrenia have shown reductions in time to recurrence, a decrease in the positive and negative symptoms of schizophrenia, and improvements in Clinical Global Impression Scale, Young Mania Rating Scale, and HAM-D scores. The following are the hypotheses:

  • Omega 3 fatty acids will be superior to placebo in the acute treatment of global autism.
  • Omega 3 fatty acids will be superior to placebo in improving aggression and irritability associated with autism.
  • Omega 3 fatty acids will be superior to placebo in improving functional ability.

Full description

This study is an innovative treatment approach to autism. It adapts a promising adjunct therapy for bipolar disorder and schizophrenia to a new population, that of children and adolescents with autism. It will analyze the possible relationship between dosage of omega 3 fatty acids and treatment outcomes. Finally, it will attempt to identify which specific subgroups of subjects will respond to this intervention, which components and associated features are most responsive and whether this impacts subjects' quality of life. The data generated by this study is intended to support the rationale for a full scale, large multi-site clinical trial.

Enrollment

17 patients

Sex

All

Ages

5 to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Child/Teen has autism.
  • He/She is between five and seventeen years of age.
  • He/She is not in the hospital.
  • He/She has a parent or legal guardian who is willing and able to sign the informed consent.

Exclusion criteria

  • Child/Teen has been diagnosed with a psychotic disorder (such as schizophrenia) or a mood disorder, including depression or bipolar disorder (manic depression).
  • He/She has caused visible harm to him/herself or is at risk for suicide.
  • He/She has an active seizure disorder or epilepsy (seizures within the past year).
  • He/She has an unstable medical illness, including heart disease.
  • He/She has experienced brain injury.
  • He/She has a history of diabetes.
  • He/She has a history of prior treatment with Omega 3 Fatty Acids.
  • He/She lives in a far away area and/or does not have regular access to transportation to the clinical facility.
  • A pregnant female or unwilling to use acceptable contraception if sexually active.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

17 participants in 2 patient groups, including a placebo group

Omega 3 fatty Acids, drug
Active Comparator group
Description:
Omega 3 Fatty acids will be dispensed to subjects in the active experimental group of the study.
Treatment:
Drug: Omega 3 fatty acids
Placebo
Placebo Comparator group
Description:
The placebo will be dispensed to subjects in the control group
Treatment:
Other: Placebo

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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