Retrospective Observations from a Pilot Study on the Feasibility and Safety of Medication Reduction or Withdrawal in Children with Autism Spectrum Disorder Taking Cannabidiol-Rich Oil

Background: Due to the limited efficacy ofcurrent treatments for Autism Spectrum Disorder (ASD), a high proportion of families turn to alternative or unregulated interventions, including medicinal Cannabis-derived products. Interest has grown in exploring the potential of cannabidiol (CBD)-based preparations as adjunctive or alternative treatments for managing core and associated symptoms of ASD. Purpose: To explore whether a CBD-rich oil provided by a Brazilian civil association for therapeutic cannabis access might be used safely alone or as adjunct, and could allow for the reduction of other medications in children with ASD. Study design: Retrospective analysis of an open-label pilot study. Methods: Thirty children with ASD aged 2–15 years old were enrolled. The feasibility, safety, and preliminary effects of medication reduction or withdrawal alongside a 24-week administration of a CBD-rich oil (CBD: delta-9-tetrahydrocannabinol -THC- ratio 14.5:1) was assessed. Results: Twenty-seven participants completed the study. Sixteen participants reduced or withdrew medications under supervision; fourteen remained on or off medication. Mild side effects like increased appetite and nervousness occurred without clear differences between groups. Two participants with epilepsy experienced seizure recurrence following the tapering of valproic acid and risperidone, respectively. Exploratory observations suggested potential improvements in ASD symptoms, parenting stress, and neuropsychiatric evaluations across participants. Conclusions: The use of CBD-rich oil alongside supervised medication tapering maybe tolerated in some children with ASD. However, the study is limited by the retrospective design, small sample size, and lack of a placebo control. Careful clinical monitoring remains essential, particularly in children with epilepsy. Further randomized controlled trials are needed to investigate potential therapeutic roles, optimal dosing strategies, and long-term safety of CBD as an adjunctive or alternative treatment in ASD.

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Publication Details

Journal
Clinical Neuropsychopharmacology and Addiction
Published
2025-10-31
DOI
https://doi.org/10.53941/cna.2025.100007
Primary Topic
Cannabis and Cannabinoid Research
Type
article
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article

Retrospective Observations from a Pilot Study on the Feasibility and Safety of Medication Reduction or Withdrawal in Children with Autism Spectrum Disorder Taking Cannabidiol-Rich Oil

Rafael Mariano de Bitencourt, Kelser de Souza Kock, Linério Ribeiro de Novais Júnior, Paulo César Trevisol Bittencourt et al.
Clinical Neuropsychopharmacology and Addiction
Cannabis and Cannabinoid Research
article

Retrospective Observations from a Pilot Study on the Feasibility and Safety of Medication Reduction or Withdrawal in Children with Autism Spectrum Disorder Taking Cannabidiol-Rich Oil

Rafael Mariano de Bitencourt, Kelser de Souza Kock, Linério Ribeiro de Novais Júnior, Paulo César Trevisol Bittencourt, RAQUEL ALBERTI, Antonio Inserra, Alysson Madruga de Liz, Antonella Campanale, Diego Morais Gomes
article en

Abstract

Background: Due to the limited efficacy ofcurrent treatments for Autism Spectrum Disorder (ASD), a high proportion of families turn to alternative or unregulated interventions, including medicinal Cannabis-derived products. Interest has grown in exploring the potential of cannabidiol (CBD)-based preparations as adjunctive or alternative treatments for managing core and associated symptoms of ASD. Purpose: To explore whether a CBD-rich oil provided by a Brazilian civil association for therapeutic cannabis access might be used safely alone or as adjunct, and could allow for the reduction of other medications in children with ASD. Study design: Retrospective analysis of an open-label pilot study. Methods: Thirty children with ASD aged 2–15 years old were enrolled. The feasibility, safety, and preliminary effects of medication reduction or withdrawal alongside a 24-week administration of a CBD-rich oil (CBD: delta-9-tetrahydrocannabinol -THC- ratio 14.5:1) was assessed. Results: Twenty-seven participants completed the study. Sixteen participants reduced or withdrew medications under supervision; fourteen remained on or off medication. Mild side effects like increased appetite and nervousness occurred without clear differences between groups. Two participants with epilepsy experienced seizure recurrence following the tapering of valproic acid and risperidone, respectively. Exploratory observations suggested potential improvements in ASD symptoms, parenting stress, and neuropsychiatric evaluations across participants. Conclusions: The use of CBD-rich oil alongside supervised medication tapering maybe tolerated in some children with ASD. However, the study is limited by the retrospective design, small sample size, and lack of a placebo control. Careful clinical monitoring remains essential, particularly in children with epilepsy. Further randomized controlled trials are needed to investigate potential therapeutic roles, optimal dosing strategies, and long-term safety of CBD as an adjunctive or alternative treatment in ASD.

Clinical Neuropsychopharmacology and AddictionVol. 1(1)
Universidade do Estado de Santa Catarina (BR), University of Chieti-Pescara (IT), Universidade Federal de Santa Catarina (BR), Universidade do Sul de Santa Catarina (BR), Instituto Federal de Educação, Ciência e Tecnologia de Santa Catarina (BR), McGill University (CA)
Openalex Percentile: Top 64%
Cannabis and Cannabinoid Research
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