Abstract
This double-blind and placebo-controlled clinical trial in autistic children had three objectives: (a) to replicate earlier findings that haloperidol administration is associated with a significant reduction of behavioral symptoms; (b) to further assess its safety when given on a short-term basis: and (c) to assess whether it has an effect on discrimination learning. Forty-five children, 2.02 to 7.58 years old (M=4.49), completed this crossover design, with random assignment to treatment sequences. Haloperidol was shown to be a powerful therapeutic agent when administered for 4 weeks and free of side effects; at doses ranging from 0.25 to 4.0 mg/day (M=0.844), there was a clinically and statistically significant reduction of a variety of symptoms. Under the given conditions, the children failed to learn on either haloperidol or placebo.
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This work was supported in part by National Institute of Mental Health grant MH 32212 and was aided by Social and Behavioral Sciences Research grant 12-108 from March of Dimes Birth Defects Foundation (Dr. Campbell). The authors thank Dr. Dennis Grega and Mr. Charles W. Hamilton for participating in this research; Dr. Michael Palij for analyzing the discrimination learning data; Dr. John E. Overall for statistical consultation; and McNeil Pharmaceutical for Haldol and matching placebo tablets.
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Anderson, L.T., Campbell, M., Adams, P. et al. The effects of haloperidol on discrimination learning and behavioral symptoms in autistic children. J Autism Dev Disord 19, 227–239 (1989). https://doi.org/10.1007/BF02211843
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DOI: https://doi.org/10.1007/BF02211843